Scholarly article on topic 'Diterpenoids of terrestrial origin'

Diterpenoids of terrestrial origin Academic research paper on "Chemical sciences"

0
0
Share paper
Academic journal
Nat. Prod. Rep.
OECD Field of science
Keywords
{""}

Academic research paper on topic "Diterpenoids of terrestrial origin"

NPR

ROYAL SOCIETY OF CHEMISTRY

REVIEW

View Article Online

View Journal

CrossMark

dick for updates

Cite this: DOI: 10.1039/c4np00108g

Diterpenoids of terrestrial origin

James R. Hanson*

Received 27th June 2014 DOI: 10.1039/c4np00108g www.rsc.org/npr

Covering: January to December 2013. Previous review, Nat. Prod. Rep., 2013, 30, 1346-1356

This review covers the isolation and chemistry of diterpenoids from terrestrial as opposed to marine sources and includes labdanes, clerodanes, abietanes, pimaranes, kauranes, cembranes and their cyclization products. There are 179 references.

1 Introduction

2 Acyclic and related diterpenoids

3 Bicyclic diterpenoids

3.1 Labdanes

3.2 Halimanes and clerodanes

4 Tricyclic diterpenoids

4.1 Pimaranes

4.2 Abietanes and their relatives

5 Tetracyclic diterpenes

6 Macrocyclic diterpenoids and their cyclization products

7 Miscellaneous diterpenoids

8 References

1 Introduction

This report follows the pattern of its predecessors1 covering the identification and chemistry of diterpenoids of terrestrial as opposed to marine origin. The latter are thoroughly reviewed in the articles on marine natural products.2 In many cases diter-penoids from marine sources have carbon skeletons that are very different from those of terrestrial origin. The commercial production of stevia extracts as non-nutritive sweeteners has led to a number of studies on the chemistry of its diterpenoid aglycone, steviol, with the objective of exploring the biological activity of the related kauranoid diterpenes.116'117

A number of reviews have appeared on the constituents of various diterpenoid bearing plant species including Salvia,3 Chloranthus,4 Xylopia,5 and Pinus species.6

2 Acyclic and related diterpenoids

An increasing number of dimeric diterpenoids have been identified and which are formed from two known compounds. The aphanamenes A and B are dimers which were isolated7 from a South Eastern Asian tree, Aphanamixis grandiflora

University of Sussex, Department of Chemistry, Brighton, Sussex, UK

(Meliaceae). They showed a significant inhibition of NO production and may be formed by a (4 + 2) cycloaddition of two known diterpene monomers, melidianolic acid A and nemor-alisin C.

3 Bicyclic diterpenoids

3.1 Labdanes

A diterpene synthase from the clary sage, Salvia sclarea, has been identified8 which catalyses the cyclization of geranylger-anyl diphosphate to (8R)-hydroxycopalyl diphosphate. The ready availability of a number of labdanes such as manool, larixol and sclareol has led to their use as chiral starting materials for synthesis. The application of manool in the partial synthesis of sesquiterpenes and diterpenes has been reviewed.9 The anti-malarial activity of 13-benzyl-15,16-bisnorlabdanes derived from manool has been examined.10 The synthesis of the drimane sesquiterpenoids (—)-albrassitriol and its 6-epimer from larixol has been reported,11 whilst larixol and sclareol provided the starting materials for the synthesis of some dri-manes including 6-ketoeuryfuran and 6-ketowinterin.12 Modification of the side chain of communic acid 1, which is readily obtained from Juniper berries, has been used to confirm the structure of some labdanes.13 The total synthesis of the tetra-norlabdane asperolide C by an iridium catalysed polyene cyclization has been described.14

Variations between the labdane, pimarane and abietane components of the needles and twigs of different populations of

Review

the Siberian dwarf pine, Pinus pumila, have been reported.15 Sclareol was identified16 in an examination of the bio-active constituents of Salvia chrysophylla (Lamiaceae), whilst cis-sclareol with an unusual cis A/B ring junction was amongst the anti-mycobacterial labdanes obtained17 from Leucas stelligera (Lamiaceae). The labdorffianic acids A and B (e.g. A, 2) were isolated18 along with some atisane diterpenoids, xylodiol 7-acetate and xylopinone, from the tree Xylopia langsdorffiana (Annonaceae). The anti-bacterial activity of Alpinia nigra (Zin-giberaceae) has been associated19 with the presence of some known labdane 15,16-dialdehydes. The pahangensins A and B are anti-bacterial dimeric and monomeric labdanes, respectively, which were obtained20 from another wild ginger, Alpinia pahangensis.

The cytotoxic biological activity of andrographolide and its derivatives has continued to attract attention and a number of aspects of its chemistry have been explored in this context.27-30 The tumour inhibitory effects of grindelic31 and imbricatolic32 acids have been examined. Andalusol has been shown to protect mitochondria from deleterious changes induced by hydrogen peroxide and other effects associated with age-related neuro-degenerative diseases.33

Further labdanes have been isolated from Vitex species (Verbenaceae) which have been used in Chinese traditional medicine, including the vitextrifolins A-G (e.g. A, 6) from V. trifolia34 and viterotulin B 7 from V. rotundifolia.35 The metabolic diversity of Coleus forskohili (Lamiaceae) on the Indian sub-continent has been investigated36 in the context of forskolin production.

The 12(R)-12-hydroxylabda-8(17),13(16),14-trien-18- and 19-oic acids have been identified21 as constituents of the wood of the Taiwanese conifer, Cunninghamia konishii (Taxodiaceae). Examination of the stems of Mallotus japonicus (Euphorbia-ceae), which has been used in Chinese traditional medicine, afforded22 the mallonicusins A-H (e.g. A, 3). Extraction of the fruits of Amomum kravanh (Zingiberaceae), a Chinese traditional medicine which is used to treat stomach disorders, yielded23 the labdane 4 together with some isospongiane diterpenoids known as the kravanhins A-C which possess a cis B/C ring junction. Further labdanes have been isolated24" from Leonotis leonurus, whilst a 15,16-dinorlabdane (5) with an unusual 13,14-acetylene has been identified246 in Leonurus japonicus (Lamiaceae). A series of ent-3,4-seco-labdan-3-oic acids have been obtained25'26 from the leaves of Callicarpa nudiflora (Verbena-ceae). They were shown to have anti-inflammatory activity due to inhibition of NO production.

3.2 Halimanes and clerodanes

The scopariusins A-C (e.g. A, 8) together with the ent-halimane isoscoparins (e.g. M, 9) have been obtained37 from Isodon scoparius (Lamiaceae). The rearranged ent-halimanes may be formed by the migration of the C-9:C-10 bond to C-11. Ent-halimic acid has been used38 as the starting material for a synthesis of the anti-tumour indole:sesquiterpene alkaloid, 12-epi-ent-pentacyclindole.

The structures and biological activity of the clerodanes have made them attractive synthetic targets. A Diels-Alder cycloaddition has been explored39 in the construction of the decalin core of the clerodanes. The structural features which contribute to the selective binding of the psychoactive salvi-norin A to the k-opioid receptor have continued to stimulate investigations into its chemistry and detection.40-42 The bio-

transformation of clerodanes by Rhizopus stolonifer has been reported.43

Further investigations of Scutellaria barbata (Lamiaceae) have afforded44 the clerodanes scutebatas P-R (e.g. P, 10), whilst scopariusic acid from Isodon scoparius has been shown45 to be a meroditerpenoid containing a cyclobutane ring formed by the cycloaddition of the 13E double bond of isoscoparin P (11) to trans-4-hydroxycinnamate esters.

Amongst the cis-clerodanes that have been isolated from Chinese liverworts are the ciliatolides A-D (e.g. A, 12) from Scapania ciliata (scapaniaceae)46 and the cephaloziellins A-F (e.g. A, 13) from Cephaloziella kiaeri.47 Further investigations of the woody climber Tinospora cordifolia (Menispermaceae) afforded48 tincordin 14 which has insect anti-feedant activity, whilst the caseabalansins are a group of cytotoxic clerodanes which were obtained49 from Casearia balansae (Flacourtiaceae). Some of these clerodanes possess an unusual C-2:C-19 oxygen bridge.

The amomaxins (e.g. A, 19) from Amomum maximum (Zingi-beraceae) have an unusual skeleton, which may be derived53 from a labdane, in which the nine-membered ring is formed by oxidative cleavage of the C-8:C-9 bond and an aldol condensation between C-17 and C-12.

Examination of Mexican Salvia species led50 to the isolation of the sepulturins A-F (e.g. A, 15) from S. shannoni and a revision of the structure of infuscatin to that of 16. The aerial parts of S. microphylla contained51 the unusual rearranged clerodane microphyllandiolide 17. The laevinoids A and B (e.g. A, 18) isolated from Croton laevigatus (Euphorbiaceae) were also assigned52 an unusual clerodane skeleton containing a cyclopropane ring.

4 Tricyclic diterpenoids

4.1 Pimaranes

The norditerpenoid 8b-hydroxy-18-nor-4,15-isopimaradien-3-one has been isolated54 from Euonymus grandiflorus (Celas-traceae). Investigation of the Chinese liverwort, Plagiochila pulcherrima yielded55 pimara-8(14),15-dien-11a-ol and the corresponding 1b,11a- and 7b,11a-diols, whilst the more highly oxygenated pedinophyllols A-J (e.g. A, 20) were obtained56 from Pedinophyllum interruptum. Further studies57 of the Chinese drug Gua-jin-ban, derived from Excoecaria acerifolia (Euphorbiaceae), afforded the excoecarins F-H (e.g. F, 21) whilst the 3,4-seco-ent-isopimarane agallochaexcoerin D 22 was obtained58 from the wood of the Indian mangrove plant E. agallocha. A study of the use of fungal pathogens as biocontrol agents of weeds such as 'fat-hen' (Chenopodium album) has led59 to the isolation of chenopodolin 23 from Phoma chenopodicola. This is

Review

a phytotoxic metabolite of this pathogen of the weed. The xylarianes are pimaranes which have been isolated60 from Xylaria species. The larvicidal activity of sphaeropsidin A against Aedes aegypti, a mosquito that is a vector of dengue fever, has been reported.61 An unusual 1:10-cyclopropyl-ent-7,15-pimaradiene 24 has been found62 in Calceolaria talcana (Scro-phulariaceae). It has tyrosinase inhibitory activity. Since an abietatriene with the normal A/B stereochemistry was reported from the same plant, further evidence for the stereochemistry of 24 is required. The euphebracteolatins A and B (e.g. A, 25) are rosanes which were isolated63 from Euphorbia ebracteolata. However, there was little evidence for the absolute stereochemistry that was assigned to them.

been used as a sedative and some of the aquilarabietic acids A-J (e.g. A, 29) that it contains have been shown71 to be active as anti-depressants.

The majusanins A-C and majusanic acid E 30 have been obtained72 from the roots of Illicium majus (Schisandraceae) whilst the jiadifenoic acids isolated73 from the roots of I.jiadi-fengpi have anti-viral activity. These include an unusual spiranic dimer, jiadifenoic acid A (31), which is formed by a Diels-Alder reaction of a spirodienone (32) arising by rearrangement of an 8a,9a-epoxide. Acanthopanolide B 33 is a highly-oxygenated abietane obtained74 from the roots of Acanthopanax brachypus (Araliaceae).

4.2 Abietanes and their relatives

The oxidative enzyme system CYP76AH4, which catalyses the conversion of miltiradiene to abietatriene and ferruginol, has been characterized64 and a related system CYP76AH1 has been expressed65 in yeast in order to produce ferruginol from miltiradiene in the context of tanshinone biosynthesis. Resin acid conversions with CYP1O5A1 from Streptomyces griseus have also been explored.66

The abietanes that are found in Pinus mugo have been considered67 as markers for these trees. Further abietanes including the triptobenzene R 26 have been isolated68 from the roots of the 'Thunder God Vine' (Tripterygium wilfordii, Celas-traceae), a plant which is used in traditional Chinese medicine for the treatment of cancer. The evolutchuols A-E (e.g. A, 27) were obtained69 from the Okinawan shrub, Euonymus lutch-uensis (Celastraceae). Amongst the abietanes isolated70 from the Thai medicinal herb Hyptis suaveolens (Lamiaceae) were iso-suaveolic acid 28 and 8a,9a-epoxysuaveolic acid. Chinese eaglewood (Chenxiang, Aquilaria sinensis, Thymelaceae) has

New quinones continue to be isolated from Salvia species such as S. corrugata75a and xantoquinone, 5a,6a-dimethoxy-abieta-8,12-diene-7,11,14-trione, has been isolated from S. xanthocheila75b whilst further degraded abietanes have been obtained from S. przewalskif6 and cell cultures of S. miltiorrhiza.77 Examination of Isodon lophanthoides var. gerardianus (Lamiaceae), which is used as 'xihuangcao' in Chinese herbal beverages, has afforded a number of abietanes including 11,12,15-trihydroxy-7-oxoabieta-8,11,13-trien-7-one78 and various relatives known as the graciflorins.79 A rearrangement involving the

View Article Online NPR

cleavage of ring A leads to the structure of graciflorin D 34. Rearranged abietanes in which a methyl group has migrated from C-4 to C-3, and in which the C-13 isopropyl group has been converted to an n-propyl group have been isolated from Cler-odendrum trichotomum (Lamiaceae).80 Other abietanes, the ent-abierubesins, have been isolated from I. rubescens,81 and iso-abietenin A 35 has been isolated from I. tenuifolius.82

Salicassin is a chalcone:diterpene (sugiol) adduct which was obtained83 from the root bark of Maytenus salicifolia (Celas-traceae). A giant invasive Brazilian water fern, the kariba weed, Salvinia molesta (Salviniaceae), was the source of salviniol 36 which possesses a ferruginol-menthane coupled skeleton and showed activity against several human cancer cell lines.84 Tri-chotomone is a dimeric abietane which was isolated85 from the roots of Clerodendrum trichotomum (Lamiaceae).

Cassanes are common constituents of Caesalpinia (Fabaceae) species and a number of new examples have been isolated including the caesalpins (e.g. A, 38)97 and some 16 / 12 lactones such as the caesalpinolides (e.g. F, 39) from C. minax98 and C. crista." Ring C has been cleaved in an unusual manner to afford the caesalminaxins (e.g. A, 40) which were also obtained100 from C. minax. The voulkensins (e.g. C, 41) are 11-oxocassanes that were obtained101 from C. volkensis, a plant which has anti-malarial activity. The caesanines (e.g. A, 42), which were isolated102 from the Chinese herb C. sappan, have a nitrogen bridge across ring A which is reminiscent of the tetracyclic diterpene alkaloids. Schaffnerine is a dimeric 7,8-seco-cassane diterpene which has been obtained103 from the Mexican tree, Acacia schaffneri (Leguminosae). The total synthesis of cassaine from (+)-carvone has been reported.104

The oxidation of the methyl ether of 6,7-dehydroferruginol with dimethyldioxirane has been examined86 in the context of the synthesis of more highly oxidized abietanes. A series of dehy-droabietic acid, dehydroabietylamine and maleopimaric acid derivatives have been synthesized and their activity against human cancer cell lines has been assessed.87-91 In another study of the abietanes derived from Salvia and Plectranthus species, taxodone (37) proved to be particularly active against human tumour cells.92 Some tanshinones from S. miltiorrhiza have been shown93 to inhibit the action of the carboxyesterases in the liver which compromise the activity of pro-drugs, whilst taxusabietane C from Taxus wallichiana is an inhibitor of lipoxygenase.94 Some arylamine fluorescent cell probes containing dehydroabietic acid units have been synthesized.95 An enantioselective synthesis has been reported96 of the pygmaeocins A and B which are irregular abietanes in which C-19 has migrated from C-10 to C-5.

A number of degraded diterpenes have been reported which may have their origin in cassanes or cleistanthanes. These include the trigophyxins J-N from Trigonostemon xypho-phylloides (Euphorbiaceae)105 and an unusual phenylacetylene, phyllanflexoid A (43) from Phyllanthus flexuosus (Euphorbiaceae) roots. This plant also contained a related cleistanthol.106 The bicelaphanols A (44), isolated as two atropisomers, and fimbricalyx A are norditerpene dimers which were obtained from the Oriental bittersweet vine Celastrus orbiculatus (Celastraceae)107 and Strophioblachia fimbricalyx (Euphorbiaceae).108

Review

Some further icetexanes have been isolated, including foki-hodgin J (45) from the Chinese medicinal plant Fokienia hodg-insii (Cupressaceae),109 perovskatone A (46) from Perovskia atriplicifolia (Lamiaceae),110 and the dimeric obtusinones D and E from Premna obtusifolia (Lamiaceae) roots.111 Some synthetic studies in this area have been reported.112

activity of medicinal plants. These include 18,19-dihydroxy-ent-kaur-16-en-3-one from Euryops arabicus (Asteraceae),126 17-hydroxy-ent-kaur-15-en-19-al from the 'Custard-apple tree' (Annona squamosa, Annonaceae)127 and 11a-hydroxyleukamenin E (47) from Salvia cavaleriei (Lamiaceae).128 Some epoxides obtained from the ent-kaurenoic acids of Wedelia paludosa have shown good activity against chloroquine resistant strains of Plasmodium falciparum,129 whilst some 19-nor ureas derived from 11ß,15ß-dihydroxy-eni-kaurenoic acid were selective inhibitors of 11ß-hydroxysteroid dehydrogenase,130" and line-arol and sidol have been shown130b to exert a cytoprotective effect against oxidative injury.

The taiwania quinones possess a 6:5:6 ring system in which the five-membered ring B carries an aldehyde group. A number of syntheses of these diterpenes, including the ring contraction of sugiol methyl ether, have been reported.113-115

5 Tetracyclic diterpenes

The approval of stevia as a non-nutritive sweetener for human consumption by the European Food Safety Authority in 2011 has meant that the aglycone steviol (ent-13-hydroxykaur-16-en-19-oic acid) and its beyerane Wagner-Meerwein rearrangement product, isosteviol, have become readily available for chemical transformations. The steviol glycosides found in Stevia rebaudiana [Asteraceae (Compositae)] and their metabolism, and the use of isosteviol as a starting material for a variety of transformations have been reviewed.116'117 Variations in the steviol content and major steviol glycosides isolated from S. rebaudiana grown in different regions and under different photoperiods have been documented.118 The transglycosylation of stevioside to improve its properties as a sweetener has been examined.119 A series of Beckmann rearrangements and fragmentation reactions of the bicyclo[3,2,1]octane ring system of steviol and isosteviol have been described.120 Some derivatives of isosteviol with vasorelaxant properties have been prepared.121 The cytotoxic and apoptosis-inducing activities of various steviol and isosteviol derivatives have been examined, including a number in which a heterocyclic ring has been added to ring

D 122-124

Seasonal variations in the formation of grandifloric acid derivatives by Mikania (Asteraceae) species have been noted.125 A number of kaurenes have been associated with the cytotoxic

The Vietnamese plant Croton tonkinensis (Euphorbiaceae) is a rich source of diterpenoids, some of which have antiinflammatory activity. New isolates include the crotonkinins C-J (e.g. C, 48).131 Further ent-kaurenes, including 49, have been obtained132 from Pteris semipinnata, whilst the graecu-mosides A and B (e.g. A, 50) are glycosides which were isolated133 from fenugreek seeds (Trigonella foenum-graecum, Fabaceae).

The investigations of Chinese Isodon species (Lamiaceae) have yielded over 600 diterpenoids, many of which possess cytotoxic and other medicinal properties. Further examples include 3a,l4b,16a-trihydroxy-ent-kaurane from I. japonicus,134 the rabdonervosins G-J (e.g. G, 51) from I. nervosus,135 the isorosthins A-P (e.g. the 20-norenmein isorosthin A, 52) from I. rosthornii,136 sculponin M (53) from I. sculponeatus,137 and effusanin F (54) from Rabdosia (Isodon) serra.138 The latter showed anti-bacterial activity. The chemistry of oridonin, which is one of the more readily available members of this series, has been explored in the context of anti-tumour structure-activity

relationships.139'140

View Article Online NPR

carbon skeleton, is a more highly degraded example that was isolated152 from R. molle.

Further total syntheses of ent-kaurene and ent-beyerane diterpenoids have been reported.141'142 The transformation of ent-kaurenoic and trachylobanic acids from sunflower waste, using fluorosulfonic acid to form the carbocation that links the families of tetracyclic diterpenes, has led to the synthesis of some atisane diterpenes.143 The atisane diterpenoids, xylodiol acetate and xylopinone have been isolated18 from Xylopia langsdorffiana (Annonaceae).

An interesting ring-contraction reaction of 7-oxoditerpenes with diacetoxyiodobenzene has afforded144 some gibberellin analogues (e.g. 55) in the ent-kaurene, ent-trachylobane and ent-atisane series. The characterization of the gibberellin oxidases from cucumber, Cucumis sativus, has been reported.145 The microbiological transformation of 15a-hydroxy-ent-kaur-9(11),16-dienes by Fusarium (Gibberella) fujikuroi has shown146 that a 9(11) double bond impedes hydroxylation at C-7 and hence ring contraction, but not 6,7-dehydrogenation and the formation of the kaurenolides. Since the gibberellin plant hormones occur in very small amounts in plants, their separation and determination has continued to be an analytical challenge and further refinements to methods have been described.147 Pharbinilic acid (56) is a 9-epiallogibberic acid derivative which was obtained148 from Morning Glory (Pharbitis nil, Convolvulaceae).

Grayane diterpenoids are characteristic diterpenoids of Rhododendron and Pieris (Ericaceae) species. Micranthanone A (57) is an ent-beyerane analogue which was isolated149 from Rhododendron micranthum. A number of 3,4-seco-grayanes including the pierisformotoxins A-D (e.g. A, 58) from Pieris formosa150 and their chlorine-containing relatives, the neo-pierisoids A and B from P. japonica, have insect anti-feedant activity.151 Mollolide A (59), with a 1,10:2,3-diseco-grayane

6 Macrocyclic diterpenoids and their cyclization products

The identification of bacterial diterpene cyclases that synthesize the cembrane skeleton153 and precursors to the fusicoccanes154 have been reported. Nephthenol 15-O-b-D-quinovoside is a cembrane glycoside which was obtained155 from Asterothamnus central-asiaticus (Asteraceae). Strategies for the synthesis of cembranolides have been examined.156 Some casbane diterpe-noids have been isolated157 from the roots of Euphorbia pekinensis.

The Canadian yew, Taxus canadensis, is a prolific source of taxanes. A review listing their isolation and discussing their chemistry has appeared.158 A short enantioselective synthesis of a taxol ring A fragment has been reported.159

Diterpenoids of the lathyrane, tigliane, ingenane, daphnane and related carbon skeletons possess a range of biological activities, including interaction with protein kinase C which plays a role in regulating cellular growth and differentiation. Diterpenoids with these skeletons are characteristic constituents of plants of the euphorbiaceae and thymelaceae, a number of which are used in Chinese traditional medicine. The medicinal properties and phytochemistry of several Jatropha species have been reviewed.160 The ekanpenoids (e.g. A, 60) are norlathyranes which were isolated161" from the roots of the Chinese herbal medicine Euphorbia kansuensis, whilst further investigations of E. micractina afforded1616 the euphactins (e.g. E, 61). Some jatrophanes have been obtained162" from E. den-droides, whilst the sikkimenoids (e.g. A, 62) were isolated1626 from E. sikkimensis. The crotocascarins (e.g. A, 63) were isolated163 from Croton cascarilloides (Euphorbiaceae) whilst further cytotoxic phorbol esters have been obtained164 from C. tiglium. The tigliane stelleracin A (64) from the Nepalese medicinal plant Stellera chamaejasme (Thymelaceae) was reported165 to show anti-HIV activity. A number of tigliane and daphnane esters showing inhibitory activity against human cancer cell lines have been isolated166-168 from the flower buds of Daphne genkwa (Thymelaceae), which are used in Chinese traditional medicine. These include the daphneresinferins (e.g.

Review

A, 65).168 Acerifolin A is a tigliane which was obtained169 from Excoecaria acerifolia (Euphorbiaceae), whilst the cyclomyrsinol structure 66 has been assigned170 to an immunosuppressive diterpenoid from Euphorbia kopetdaghi.

The 13C NMR spectra of the daphnane diterpenoids have been reviewed.171 The pharmaceutical potential of phorbol esters obtained from Jatropha curcas oil has been examined172 in the context of their relationship with prostratin. Some structure-activity relationships amongst ingenol 3-angelate analogues in the treatment of actinic keratosis and non-melanoma skin cancer have been explored.173 Approaches to the synthesis of the tigliane-daphnane ring system have been reported.174

The roussoeliols A and B (e.g. A, 67) are fusiccane metabolites of the fungus, Roussella hysteroides.175

The trigoxyphins O-T from Trigonostemon xyphylloides (Euphorbiaceae) have been assigned179 structures (e.g. O, 69) which may be derived from two degraded diterpenes.

7 Miscellaneous diterpenoids

The total synthesis of the cyanthiwigins A, C, G and H has been described.176 Further prenylated sesquiterpenes have been reported including the boscartols (e.g. A, 68) which are prenyl aromadendranes that were isolated177 from frankincense resin, Boswellia carterii (Burseraceae). The serrulatane leubethanol has been synthesized178 from isopulegol. This anti-bacterial compound from Leucophyllum frutescens has potentially useful activity against resistant strains of bacteria.

8 References

1 J. R. Hanson, Nat. Prod. Rep., 2013, 30, 1346-1356.

2 J. W. Blunt, B. R. Copp, R. A. Keyzers, M. H. G. Munro and M. R. Prinsep, Nat. Prod. Rep., 2014, 31, 160-258.

3 Y. B. Wu, Z. Y. Ni and Q. W. Shi, Chem. Rev., 2012, 112, 5967-6026.

4 Y. J. Xu, Chem. Biodiversity, 2013, 10, 1754-1773.

5 I. C. Moreira, N. F. Roque, W. Vilegas, C. A. Zalewski, J. H. G. Lago and M. Funasaki, Chem. Biodiversity, 2013, 10, 1921-1943.

6 B. Li, Y.-H. Shen, Y.-R. He and W.-D. Zhang, Chem. Biodiversity, 2013, 10, 2133-2160.

7 H.-J. Zhang, J. Luo, S.-M. Shan, X.-B. Wang, J.-G. Luo, M.-H. Yang and L.-Y. Kong, Org. Lett., 2013, 15, 5512-5515.

8 N. Gunnewich, Y. Higashi, X. Feng, K.-B. Choi, J. Schmidt and T. M. Kutchan, Phytochemistry, 2013, 91, 93-99.

9 (a) F. J. Salazar and J. E. Villamizar, J. Chem. Res., 2013, 37, 1-5; (b) F. J. Salazar and J. E. Villamizar, J. Chem.. Res., 2013, 37, 63-70.

10 F. J. Salazar, A. Quintero, N. G. Dominguez, J. L. Concepcion, M. E. Acosta, E. Tropper and J. E. Villamizar, J. Chem.. Res., 2013, 37, 657-661.

11 P. F. Vlad, A. Ciocarlan, M. Coltsa, C. Edu, A. Biriiac, A. Barba, C. Deleanu, A. Nicolescu, M. D'Ambrosio and A. de Groot, Nat. Prod. Res., 2013, 27, 809-817.

12 P. F. Vlad, A. Ciocarlan, C. Edu, A. Aricu, A. Biriiac, M. Coltsa, M. D'Ambrosio, C. Deleanu, A. Nicolescu, S. Shava, N. Vornicu and A. de Groot, Tetrahedron, 2013, 69, 918-926.

13 D.J. Mack and J. T. Njardson, Angew. Chem., Int. Ed., 2013, 52, 1543-1547.

14 O. F. Jeker, A. G. Kravina and E. M. Carreira, Angew. Chem., Int. Ed., 2013, 52, 12166-12169.

15 A. V. Shpatov, S. A. Popov, O. I. Salnikova, E. N. Schmidt, S. W. Kang, S. M. Kim and B. H. Um, Chem. Biodiversity, 2013, 10, 198-208.

16 B. Culhaoglu, G. Yapar, T. Dirmenci and G. Topcu, Nat. Prod. Res., 2013, 27, 438-447.

17 R. R. Kulkarni, K. Shurpali, V. Puranik, D. Sarkar and S. P. Joshi, J. Nat. Prod., 2013, 76, 1836-1841.

18 P. F. dos Santos, M. C. Duarte, D. A. C. Bezerra, M. d. F. Agra, J. M. Barbosa Filho, M. S. da Silva and J. F. Tavares, Helv. Chim. Acta, 2013, 96, 1085-1092.

19 S. Ghosh, K. Indukuri, S. Bondalapati, A. K. Saikia and L. Rangan, European J. Medic. Chem., 2013, 66, 101-105.

20 Y. Sivasothy, H. Ibrahim, A. S. Paliany, S. A. Alias and K. Awang, Bioorg. Med. Chem. Lett., 2013, 23, 6280-6285.

21 Y. C. Chen, Y.-C. Li, H. L. Chiu, W.-Y. Cheng, Y.-H. Hong, P. J. Sung, C. C. Kuo, B. T. Wu and Y. H. Kuo, Helv. Chim. Acta, 2013, 96, 2282-2287.

22 D.-Z. Li, C. Tang, R. J. Quinn, Y. Feng, C.-Q. Ke, S. Yao and Y. Ye, J. Nat. Prod., 2013, 76, 1580-1585.

23 H. Yin, J.-G. Luo and L.-Y. Kong, J. Nat. Prod., 2013, 76, 237242.

24 (a) H. Wu, J. Li, F. R. Fronczek, D. Ferreira, C. L. Burandt, V. Setola, B. L. Roth and J. K. Zjawiony, Phytochemistry, 2013, 91, 229-235; (b) F. Peng, L. Xiong and X. M. Zhao, Molecules, 2013, 18, 13904-13909.

25 L. Zhang, J. Huang, M.-S. Liu, C. Zhang, G. Li, K. Zhang, L. Dong and J. Wang, Heterocycles, 2013, 87, 1561-1569.

26 L. Dong, X.-P. Zhang, M.-S. Liu, Y.-M. Li, J. H. Wang and Y. Wang, J. Asian Nat. Prod. Res., 2013, 15, 30-34.

27 D. Chen, Y. Song, Y. Lu and X. Xue, Bioorg. Med. Chem. Lett., 2013, 23, 3166-3169.

28 S. Wei, Y.-B. Tang, H. Hua, E. Ohkoshi, M. Goto, L.-T. Wong, K. H. Lee and Z. Xiao, Bioorg. Med. Chem. Lett., 2013, 23, 4056-4060.

29 D. Singh and P. K. Chaudhuri, Nat. Prod. Res., 2013,27, 680683.

30 X.-W. Xiao, H.-Z. Fu, Y.-H. Luo and X.-Y. Wei, J. Asian Nat. Prod. Res., 2013, 15, 809-818.

31 G. F. Reta, A. J. Chiaramello, C. Garcia, L. G. Leon, V. S. Martin, J. M. Padron, C. E. Tonn and O. J. Donadel, European J. Medic. Chem., 2013, 67, 23-28.

32 M. W. Pertino, C. Theoduloz, M. Bastias and G. Schmeda-Hirschmann, Molecules, 2013, 18, 5936-5953.

33 E. Gonzalez-Burgos, A. I. Duarte, M. E. Carretero, P. I. Moreira and M. P. Gomez-Serranillos, J. Nat. Prod., 2013, 76, 933-938.

34 C.-J. Zheng, J.-Y. Zhu, W. Yu, X.-Q. Ma, K. Rahman and L.-P. Qin, J. Nat. Prod., 2013, 76, 287-291.

35 C. Lee, J. W. Lee, Q. Jin, H. J. Lee, S.-J. Lee, D. Lee, M. K. Lee, C.-K. Lee, J. T. Hong, M. K. Lee and B. Y. Hwang, Bioorg. Med. Chem. Lett., 2013, 23, 6010-6014.

36 E. J. Tamboli, M. Singh, Y. T. Kamal, M. Garg, R. Parveen, M. Mujeeb and S. Ahmad, Nat. Prod. Res., 2013, 27, 17371742.

37 M. Zhou, H.-C. Geng, H.-B. Zhang, K. Dong, W.-G. Wang, X. Du, X.-N. Li, F. He, H.-B. Qin, Y. Li, J.-X. Pu and

H. D. Sun, Org. Lett., 2013, 15, 314-317.

38 I. S. Marcos, R. F. Moro, I. Costales, P. Basabe, D. Diez, F. Mollinedo and J. G. Urones, Tetrahedron, 2013, 69, 7285-7289.

39 S. C. Butler and C. J. Forsyth, J. Org. Chem., 2013, 78, 38953907.

40 B. Ivanova and M. Spiteller, Med. Chem. Res., 2013, 1-14.

41 P. R. Polepally, K. White, E. Vardy, B. L. Roth, D. Ferreira and J. K. Zjawiony, Bioorg. Med. Chem. Lett., 2013, 23, 2860-2862.

42 (a) A. P. Riley, V. W. Day, H. A. Navarro and T. E. Prisinzano, Org. Lett., 2013,15, 5936-5939; (b) M. K. Paude1, O. Shirota, K. Sasaki-Tabata, H. Tanaka, S. Sekita and S. Morimoto, J. Nat. Prod., 2013, 76, 1654-1660.

43 M. I. Choudhary, M. Y. Mohamad, S. G. Musharraf,

I. Onajobi, A. Mohammad, I. Anis, M. R. Shah and Atta-ur-Rahman, Phytochemistry, 2013, 90, 56-61.

44 Y.-Y. Li, X.-L. Tang, T. Jiang, P.-F. Li, P.-L. Li and G.-Q. Li, J. Asian Nat. Prod. Res., 2013, 15, 941-949.

45 M. Zhou, H.-B. Zhang, W.-G. Wang, N.-B. Gong, R. Zhan, X.-N. Li, X. Du, L.-M. Li, Y. Li, J. Lu, J.-X. Pu and H. D. Sun, Org. Lett., 2013, 15, 4446-4449.

46 N. Liu, R.-X. Zhu, S. Wang, J.-Z. Zhang, Z.-M. Lin, R.-J. Li and H. X. Lou, Chem. Biodiversity, 2013, 10, 1606-1612.

47 R.-J. Li, R.-X. Zhu, Y.-Y. Li, J.-C. Zhou, J.-Z. Zhang, S. Wang, J.-P. Ye, Y.-H. Wang, S. L. Morris-Natschke, K.-H. Lee and H.-X. Lou, J. Nat. Prod., 2013, 76, 1700-1708.

48 A. Sivasubramanian, K. K. G. Narasimha, R. Rathnasamy and A. M. F. Oliveira Campos, Nat. Prod. Res., 2013, 27, 1431-1436.

49 B. Wang, X.-L. Wang, S.-Q. Wang, T. Shen, Y.-Q. Liu, H. Yuan, H.-X. Lou and X.-N. Wang, J. Nat. Prod., 2013, 76, 1573-1579.

50 E. Bautista, R. A. Toscano, F. Calzada, E. Diaz, L. Yepez-Mulia and A. Ortega, J. Nat. Prod., 2013, 76, 1970-1975.

Review

51 E. Bautista, R. A. Toscano and A. Ortega, Org. Lett., 2013,15, 3210-3213.

52 G.-C. Wang, H. Zhang, H.-B. Liu and J.-M. Yue, Org. Lett., 2013, 15, 4880-4883.

53 H. Yin, J. G. Luo, S. M. Shan, X. B. Wang, J. Luo, M.-H. Yang and L.-Y. Kong, Org. Lett., 2013, 15, 1572-1575.

54 C. Li, B. Li, J. Ye, W. Zhang, Y. Shen and J. Yin, Nat. Prod. Res., 2013, 27, 1716-1721.

55 S. Wang, S. S. Liu, Z. M. Lin, R. J. Li, X. N. Wang, J. C. Zhou and H.-X. Lou, J. Asian Nat. Prod. Res., 2013, 15, 473-481.

56 N. Liu, R. J. Li, X.-N. Wang, R.-X. Zhu, L. Wang, Z.-M. Lin, Y. Zhao and H.-X. Lou, J. Nat. Prod., 2013, 76, 1647-1653.

57 S. Z. Huang, Q. Y. Ma, W. W. Fang, F. Q. Xu, H. Peng,

H. F. Dai, J. Zhou and Y. X. Zhao, J. Asian Nat. Prod. Res., 2013, 15, 750-755.

58 M. G. Ponnapalli, M. Anikireddy, S. C. V. A. Rao Annam, S. Ravirala, S. Sukki and V. R. Tuniki, Tetrahedron Lett., 2013, 54, 2942-2945.

59 A. Cimmino, A. Andolfi, M. C. Zonno, F. Avolio, A. Santini, A. Tuzi, A. Berestetskyi, M. Vurro and A. Evidente, J. Nat. Prod., 2013, 76, 1291-1297.

60 P. Xu, H. You, Z. Hu, Y. Li and Y. Shen, Chinese J. Org. Chem., 2013, 33, 2618-2621.

61 A. Cimmino, A. Andolfi, F. Avolio, A. Ali, N. Tabanca,

I. A. Khan and A. Evidente, Chem. Biodiversity, 2013, 10, 1239-1251.

62 E. Munoz, J. G. Avila, J. Alarcon, I. Kubo, E. Werner and C. L. Cespedes, J. Agric. Food Chem., 2013, 61, 4336-4343.

63 S. Z. Mu, C. R. Jiang, T. Huang and X. J. Hao, Helv. Chim. Acta, 2013, 96, 2299-2303.

64 J. Zi and R. J. Peters, Org. Biomol. Chem., 2013, 11, 76507652.

65 J. Guo, Y. J. Zhou, M. L. Hillwig, Y. Shen, L. Yang, Y. Wang, X. Zhang, W. Liu, R. J. Petes, X. Chen, Z. K. Zhao and L. Huang, Proc. Natl. Acad. Sci. U. S. A., 2013, 110, 1210812113.

66 S. Janocha, J. Zapp, M. Hutter, M. Kleser, J. Bohlmann and R. Bernhardt, ChemBioChem, 2013, 14, 467-473.

67 A. Venditti, A. M. Serrilli, S. Vittori, F. Papa, M. D. Cecca, G. Ciaschetti, M. Bruno, S. Roselli and A. Bianco, Chem. Biodiversity, 2013, 10, 2091-2100.

68 J.-Y. Li, Y. Png, L.-Z. Li, P.-Y. Gao, C. Gao, S.-X. Xia and S.-J. Song, Helv. Chim. Acta, 2013, 96, 313-319.

69 Y. Inaba, T. Hasuda, Y. Hitotsuyanagi, Y. Aoyagi, N. Fujikawa, A. Onozaki, A. Watanabe, T. Kinoshita and K. Takeya, J. Nat. Prod., 2013, 76, 1085-1090.

70 S. Prawatsri, A. Suksamrarn, A. Chindaduang and T. Rukachaisirikul, Chem. Biodivsersity., 2013, 10, 14941500.

71 L. Yang, L. Qiao, C. Ji, D. Xie, N.-B. Gong, Y. Lu, J. Zhang, J. Dai and S. Guo, J. Nat. Prod., 2013, 76, 216-222.

72 Y.-D. Wang, G.-J. Zhang, J. Qu, Y.-H. Li, J.-D. Jiang, Y.-B. Liu, S.-G. Ma, Y. Li, H.-N. Lv and S.-S. Yu, J. Nat. Prod., 2013, 76, 1976-1983.

73 G.-J. Zhang, Y.-H. Li, J.-D. Jiang, S.-S. Yu, J. Qu, S.-G. Ma, Y.-B. Liu and D.-Q. Yu, Tetrahedron, 2013, 69, 1017-1023.

74 H.-B. Hu, X.-D. Zhang, H.-S. Hu and Y. Wu, Chem. Biodiversity, 2013, 10, 1623-1629.

75 (a) E. Giacomelli, S. Bertrand, A. Nievergelt, V. Zwick, C. Simoes-Pires, L. Marcourt, E. Rivara-Minten, M. Caudet, A. Bisio and J.-L. Wolfender, Phytochemistry, 2013, 96, 257-264; (b) Z. Habibi, S. Gandomkar, M. Yousefi and S. Ghasemi, Nat. Prod. Res., 2013, 27, 266269.

76 H.-L. Jiang, X.-Z. Wang, J. Xiao, X.-H. Luo, X.-J. Yao, Y.-Y. Zhao, Y.-J. Chen, P. Crews and Q.-X. Wu, Tetrahedron, 2013, 69, 6687-6692.

77 D.-W. Zhang, X. Liu, D. Xie, R. Chen, S.-J. Tao, J.-H. Zou and J. Dai, Chem. Pharm. Bull., 2013, 61, 576-580.

78 L. Yang, S. Liu, H. Wang and Y. Suo, J. Chem.. Res., 2013, 37, 28-29.

79 (a) W. Zhou, H. Xie, P. Wu and X. Wei, Food Chem., 2013, 136, 1110-1116; (b) Y. Liang, H. Xie, P. Wu, Y. Jiang and X. Wei, Food Chem., 2013, 136, 1177-1182.

80 W.-X. Wang, J. Xiong, Y. Tang, J.-J. Zhu, M. Li, Y. Zhao, G.-X. Yang, G. Xia and J.-F. Hu, Phytochemistry, 2013, 89, 89-95.

81 X. Liu, R. Zhan, W.-G. Wang, X. Du, X.-N. Li, J.-H. Yang, P. Zhang, Y. Li, J.-X. Pu, J. Z. Wu and H. D. Sun, Chem. Pharm. Bull., 2013, 61, 90-95.

82 J.-H. Yang, X. Du, F. He, H.-B. Zhang, X.-N. Li, J. Su, Y. Li, J.-X. Pu and H.-D. Sun, J. Nat. Prod., 2013, 76, 256-264.

83 C. G. Magalhaes, G. D. Fatima Silva, L. P. Duarte, I. L. Bazzocchi, A. J. Diaz, L. Moujir, M. P. Lopez, R. C. Figueiredo and S. A. Vieira Filho, Helv. Chim. Acta, 2013, 96, 1046-1054.

84 S. Li, P. Wang, G. Deng, W. Yuan and Z. Su, Bioorg. Med. Chem. Lett., 2013, 23, 6682-6687.

85 W.-X. Wang, J.-J. Zhu, Y. Zou, Z.-L. Hong, S.-T. Liu, M. Li, Y. Huang, J. Xiong, Y. Zhao, G.-X. Yang, G. Xia and J.-F. Hu, Tetrahedron Lett., 2013, 54, 2549-2552.

86 I. Cordova-Guerrero, L. S. Andres, A. E. Lea1-Orozco, J. M. Padrón, J. M. Cornejo-Bravo and F. Leon, Tetrahedron Lett., 2013, 54, 4479-4482.

87 M. Ukiya, T. Kawaguchi, K. Ishii, E. Ogihara, Y. Tachi, M. Kurita, Y. Ezaki, M. Fukatsu, Y. Kushi and T. Akihisa, Chem. Biodiversity, 2013, 10, 1260-1268.

88 X.-C. Huang, M. Wang, Y.-M. Pan, G.-Y. Yao, H. S. Wang, X.-Y. Tian, J.-K. Qin and Y. Zhang, Eur. J. Med. Chem., 2013, 67, 508-520.

89 H.-C. Huang, M. Wang, Y.-M. Pan, X.-Y. Tain, H.-S. Wang andY. Zhang, Bioorg. Med. Chem. Lett., 2013, 23, 5283-5289.

90 Z. Zhou, Z.-X. Lin, D. Liang and J.-Q. Hu, Tetrahedron, 2013, 69, 43-49.

91 G.-Y. Yao, M.-Y. Ye, R.-Z. Huang, Y.-J. Li, Y.-T. Zhu, Y.-M. Pan, Z.-X. Liao and H. S. Wang, Bioorg. Med. Chem. Lett., 2013, 23, 6755-6758.

92 O. Burmistrova, M. F. Simoes, P. Rijo, J. Quintana, J. Bermejo and F. Estevez,J. Nat. Prod., 2013, 76,1413-1423.

93 M. J. Hatfield, L. G. Tsurkan, J. L. Hyatt, C. C. Edwards, A. Lemoff, C. Jeffries, B. Yan and P. M. Potter, J. Nat. Prod., 2013, 76, 36-44.

94 I. Khan, M. Nisar, A. Zarrelli, G. D. Fabio, F. Gul, S. N. Gilani, M. R. Shaah, A. Z. Khai and H. Amin, Med. Chem. Res., 2013, 22, 5809-5813.

95 H. Gao, S. Chen, X. Rao, S. Shang and Z. Song, Bioorg. Med. Chem. Lett., 2013, 23, 2254-2259.

96 A. Obase, A. Kageyama, Y. Manabe, T. Ozawa, T. Araki, H. Yokoe, M. Kanematsu, M. Yoshida and K. Shishido, Org. Lett., 2013, 15, 3666-3669.

97 G. Ma, J. Yuan, H. Wu, L. Cao, X. Zhang, L. Xu, H. Wei, L. Wu, Q. Zheng, L. Li, J. Yang and X. Xu, J. Nat. Prod., 2013, 76, 1025-1031.

98 G. Ma, J.-Q. Yuan, L. Cao, J.-S. Yang and X.-D. Xu, Nat. Prod. Res., 2013, 27, 818-823.

99 Q.-J. Tian, Y.-H. Ou, X.-B. He, B. Liu and Y.-D. Jiang, Nat. Prod. Res., 2013, 27, 537-540.

100 Y. Zheng, S.-W. Zhang, H.-J. Cong, Y.-J. Huang and L.-J. Xuan, J. Nat. Prod., 2013, 76, 2210-2218.

101 C. O. Ochieng, L. A. O. Manguro, P. O. Owuor and H. Akala, Bioorg. Med. Chem. Lett., 2013, 23, 3088-3095.

102 J. Zhang, W. M. Abdel-Mageed, M. Liu, P. Huang, W. He, L. Li, F. Song, H. Dai, X. Liu, J. Liang and L. Zhang, Org. Lett., 2013, 15, 4726-4729.

103 J. J. Manríquez-Torres, J. M. Torres-Valencia, R. Velazquez-Jimenez, A. Valdez-Calderon, J. G. Alvarado-Rodriguez, C. M. García-Rojas and P. Joseph-Nathan, Org. Lett., 2013, 15, 4658-4661.

104 K. Ravindar, P.-Y. Caron and P. Deslongchamps, Org. Lett., 2013, 15, 6270-6273.

105 B. Yang, G.-Y. Chen, X.-P. Song, L.-Q. Yang, X.-Y. Wu, C.-R. Han, W.-H. Chen, B.-Y. Zou and X.-M. Li, Bioorg. Med. Chem. Lett., 2013, 23, 5748-5751.

106 J.-Q. Zhao, J.-J. Lv, Y.-M. Wang, M. Xu, H.-T. Zhu, D. Wang, C.-R. Yang, Y.-F. Wang and Y.-J. Zhang, Tetrahedron Lett., 2013, 54, 4670-4674.

107 L.-Y. Wang, J. Wu, Z. Yang, X.-J. Wang, Y. Fu, S.-Z. Liu, H.-M. Wang, W.-L. Zhu, H.-Y. Zhang and W.-M. Zhao, J. Nat. Prod., 2013, 76, 745-749.

108 P. Seephonkai, S. G. Pyne, A. C. Willis and W. Lie, Tetrahedron Lett., 2013, 54, 2085-2088.

109 X.-D. Wu, J. He, X.-Y. Li, L.-B. Dong, X. Gong, L.-D. Song, Y. Li, L.-Y. Peng and Q.-S. Zhao, J. Nat. Prod., 2013, 76, 1032-1038.

110 Z.-Y. Jiang, C.-G. Huang, H.-B. Xiong, K. Tian, W.-X. Liu, Q.-F. Hu, H.-B. Wang, G.-Y. Yang and X.-Z. Huang, Tetrahedron Lett., 2013, 54, 3886-3888.

111 A.-W. Salae and N. Boonnak, Tetrahedron Lett., 2013, 54, 1356-1359.

112 F. de Jesus Cortez, D. Lapointe, A. M. Hamlin, E. M. Simmons and R. Sarpong, Tetrahedron, 2013, 69, 5665-5676.

113 C. Thommen, C. K. Jana, M. Neuburger and K. Gademann, Org. Lett., 2013, 15, 1390-1393.

114 J. Deng, R. Li, Y. Luo, J. Li, S. Zhou, Y. Li, J. Hu and A. Li, Org. Lett., 2013, 15, 2022-2025.

115 M. Ozeki, M. Satake, T. Toizume, S. Fukutome, K. Arimitsu, S. Hosoi, T. Kajimoto, H. Iwasaki, N. Kojima, M. Node and M. Yamashita, Tetrahedron, 2013, 69, 3841-3846.

116 S. Ceunen and J. M. G. Guens, J. Nat. Prod., 2013, 76,12011228.

117 C. Lohoelter, M. Weckbecker and S. R. Waldvoge1, Eur. J. Org. Chem., 2013, 5539-5554.

118 (a) P. Montoro, I. Molfetta, M. Maldini, L. Ceccarini, S. Piacente, C. Pizza and M. Macchia, Food Chem., 2013, 141, 745-753; (b) S. Ceunen and J. M. C. Geuns, Phytochemistry, 2013, 89, 32-38.

119 S. Li, W. Li, Q.-Y. Xiao and Y. Xia, Food Chem., 2013, 138, 2064-2069.

120 O. E. Hutt, T. L. Doan and G. I. Georg, Org. Lett., 2013, 15, 1602-1605.

121 O. Wonganan, C. Tocharus, C. Puedsing, S. Homvisasevongsa, O. Sukcharoen and A. Suksamrarn, Eur. J. Med. Chem., 2013, 62, 771-776.

122 M. Ukiya, S. Sawada, T. Kikuchi, Y. Kushi, M. Fukatsu and T. Akihisa, Chem. Biodiversity, 2013, 10, 177-188.

123 S.-L. Zhu, Y. Wu, C.-J. Liu, C.-Y. Wei, J.-C. Tao and H.-M. Liu, Eur. J. Med. Chem., 2013, 65, 70-82.

124 S.-L. Zhu, Y. Wu, C.-J. Liu, C.-Y. Wei, J.-C. Tao and H.-M. Liu, Bioorg. Med. Chem. Lett., 2013, 23, 1343-1346.

125 S. K. V. Bertolucci, A. B. D. Pereira, J. E. B. P. Pinto, A. B. Olivera and F. C. Braga, Chem. Biodiversity, 2013, 10, 288-295.

126 W. M. Alarif, A. Abdel-Lateff, A. M. Al-Abd, S. A. Basaif, F. A. Badria, M. Shams and S. N. Ayyad, Eur. J. Med. Chem., 2013, 66, 204-210.

127 C.-X. Zhou, L.-R. Sun, F. Feng, J.-X. Mo, H. Zhu, B. Yang, Q.-J. He and L.-S. Gan, Helv. Chim. Acta, 2013, 96, 656-662.

128 H. Zheng, Q. Chen, M. Zhang, Y. Lai, L. Lei, P. Shu, J. Zhang, Y. Xue, Z. Luo, Y. Li, G. Yao and Y. Zhang, J. Nat. Prod., 2013, 76, 2253-2262.

129 R. Batista, P. A. García, M. A. Castro, J. M. Migue1 del Corral, N. L. Speziali, F. de P. Varotti, R. C. de Paula, L. F. García-Fernandez, A. Francesch, A. San Feliciano and A. B. de Oliveira, Eur. J. Med. Chem., 2013, 62,168-176.

130 (a) X. Deng, Y. Shen, J. Yang, J. He, Y. Zhao, L.-Y. Peng, Y. Leng and Q.-S. Zhao, Eur. J. Med. Chem., 2013, 65, 403414; (b) E. González-Burgos, M. E. Carretero and M. P. Gómez-Serranillos, Phytochemistry, 2013, 93,116-123.

131 P.-C. Kuo, M.-L. Yang, T.-L. Hwang, Y.-Y. Lai, Y.-C. Li, T. D. Thang and T.-S. Wu, J. Nat. Prod., 2013, 76, 230-236.

132 R. Bai, Y. Zhou, S. Deng, P.-P. Dong, B. J. Zhang, S. S. Huang, C. Y. Wang, H.-L. Zhang, Y.-Y. Zhao, L. Wang and X.-C. Ma, J. Asian Nat. Prod. Res., 2013, 15, 1107-1111.

133 X. Pang, L.-P. Kang, H.-S. Yu, Y. Zhao, C.-Q. Xiong, J. Zhang and B.-P. Ma, Nat. Prod. Res., 2013, 27, 1202-1207.

134 W. Liu, B.-L. Fan, H.-Y. Guo, Y.-L. Yuan, H.-J. Liang and S.-P. Bai, Nat. Prod. Res., 2013, 27, 1388-1392.

135 Y.-H. Gao, Z.-X. Wei, Y. Cheng, T.-H. Wang, L. Ni, X.-H. Zhou and L.-Y. Zhang, Chem. Biodiversity, 2013, 10, 1487-1493.

136 R. Zhan, X.-N. Li, X. Du, W.-G. Wang, K. Dong, J. Su, Y. Li, J.-X. Pu and H.-D. Sun, J. Nat. Prod., 2013, 76, 1267-1277.

137 H.-Y. Jiang, W.-G. Wang, M. Zhou, H.-Y. Wu, R. Zhan, X.-N. Li, X. Du, Y. Li, J.-X. Pu and H.-D. Sun, J. Nat. Prod., 2013, 76, 2113-2119.

Review

138 L. Lin, D. Zhu, L. Zou, B. Yang and M. Zhao, Food Chem., 2013, 139, 902-909.

139 D. Li, S. Xu, H. Cai, L. Pei, H. Zhang, L. Wang, H. Yao, X. Wu and J. Xu, Eur. J. Med. Chem., 2013, 59, 215-221, 322-328.

140 C. Ding, Y. Zhang, H. Chen, C. Wild, T. Wang, M. A. White, Q. Shen and J. Zhou, Org. Lett., 2013, 15, 3718-3721.

141 E. C. Cherney, J. C. Green and P. S. Baran, Angew. Chem., Int. Ed., 2013, 52, 9019-9022.

142 P. Lu, Z. Gu and A. Zakarian, J. Am. Chem. Soc., 2013, 135, 14552-14555.

143 N. Ungur, V. Kulcitki, O. Chetraru, M. Grinco and P. F. Vlad, Helv. Chim. Acta, 2013, 96, 864-871.

144 B. M. Fraga, V. Gonzalez-Vallejo, C. Bressa, R. Guillermo and S. Suarez, Tetrahedron, 2013, 69, 3002-3012.

145 M. J. P. Lange, A. Liebrandt, L. Arnold, S.-M. Chmielewska, A. Felsberger, E. Freier, M. Heuer, D. Zur and T. Lange, Phytochemistry, 2013, 90, 62-69.

146 B. M. Fraga, V. Gonzalez-Vallejo, R. Guillermo and J. M. Amaro-Luis, Phytochemistry, 2013, 89, 39-46.

147 (a) T. Urbanova, D. Tarkowska, O. Novak, P. Heddon and M. Stand, Talanta, 2013, 112, 85-94; (b) S. Liu, W. Chen, L. Qu, Y. Gai and X. Jiang, Anal. Bioanal. Chem., 2013, 405, 1257-1266.

148 K. H. Kim, S. U. Choi, M. W. Son, S. Z. Choi, J. Clardy and K. R. Lee, J. Nat. Prod., 2013, 76, 1376-1379.

149 M. Zhang, Y. Zhu, G. Zhan, P. Shu, R. Sa, L. Lei, M. Xiang, Y. Xue, Z. Luo, Q. Wan, G. Yao and Y. Zhang, Org. Lett., 2013, 15, 3094-3097.

150 W.-G. Wang, Z.-Y. Wu, R. Chen, H.-Z. Li, H.-M. Li, Y.-D. Li, R.-T. Li and H.-R. Luo, Chem. Biodiversity, 2013, 10, 10611071.

151 Y.-P. Li, X.-N. Li, L.-H. Gao, H.-Z. Li, G.-X. Wu and R.-T. Li, J. Agric. Food Chem., 2013, 61, 7219-7224.

152 Y. Li, Y.-B. Liu, J.-J. Zhang, Y.-H. Li, J.-D. Jiang, S.-S. Yu, S.-G. Ma, J. Qu and H.-N. Lv, Org. Lett., 2013,15, 3074-3077.

153 A. Meguroa, T. Tomita, M. Nishiyama and T. Kuzuyama, ChemBioChem, 2013, 14, 316-321.

154 J. Arens, B. Engels, S. Klopries, S. Jennewein, C. Ottmann and F. Schulz, Chem. Commun., 2013, 49, 4337-4339.

155 M. Todorova, A. Trendafilova, N. Javsmaa, S. Altansetseg and S. Shatar, J. Asian Nat. Prod. Res., 2013,15, 1060-1063.

156 (a) A. Saitman, S. D. E. Sullivan and E. A. Theodorakis, Tetrahedron Lett., 2013, 54, 1612-1615; (b) A. Saitman and E. A. Theodorakis, Org. Lett., 2013, 15, 2410-2413.

157 W.-W. Tao, J.-A. Duan, Y.-P. Tang, N.-Y. Yang, J.-P. Li and Y.-F. Qian, Phytochemistry, 2013, 94, 249-253.

158 Y. Li, F. Qin, S.-M. Wang, R.-X. Guo, Y.-F. Zhang, Y. C. Gu and Q.-W. Shi, Chem. Biodiversity, 2013, 10, 1729-1753.

159 S. Hirai, N. Urushizako, M. Miyano, T. Fujii and M. Nakada, Tetrahedron Lett., 2013, 54, 1888-1892.

160 C. W. Sabandar, N. Ahmat, F. M. Jaafar and I. Sahidin, Phytochemistry, 2013, 85, 7-29.

161 (a) B.-B. Zhang, Q. Jiang, Z.-X. Liao, C. Liu, S.-J. Liu, L.-J. Ji and H.-F. Sun, Chem. Biodiversity, 2013, 10, 1887-1893; (b)

Y. Tian, W. Xu, C. Zhu, S. Lin, Y. Guo and J. Shi, J. Nat. Prod., 2013, 76, 1039-1046.

162 (a) M. Jadranin, M. Pesic, I. S. Aljancic, S. M. Milosovic, N. M. Todorovic, A. Podolski-Renic, J. Bankovic, N. Tanic, I. Markovic, V. E. Vajs and V. V. Tesic, Phytochemistry, 2013, 86, 208-217; (b) D. S. Yang, Y.-L. Zhang, W.-B. Peng, L.-Y. Wang, Z.-L. Li, X. Wang, K.-C. Liu, Y.-P. Yang, H.-L. Li and X.-L. Li, J. Mater. Prod., 2013, 76, 265-269.

163 S. Kawakami, H. Toyoda, L. Harinantenaina, K. Matsunami, H. Otsuka, T. Shinzato, Y. Takeda, M. Kawahata and K. Yamaguchi, Chem. Pharm. Bull., 2013, 61, 411-418.

164 X.-L. Zhang, L. Wang, F. Li, K. Yu and M.-K. Wang, J. Nat. Prod., 2013, 76, 858-864.

165 Y. Asada, A. Sukemori, T. Watanabe, K. J. Malla, T. Yoshikawa, W. Li, X. Kuang, K. Koike, C.-H. Chen, T. Akiyama, K. Qian, K. Nakagawa-Goto, S. L. Morris-Natschke, Y. Lu and K.-H. Lee, J. Nat. Prod., 2013, 76, 852-857.

166 R. Wang, J.-Y. Li, H.-Y. Qi and Y.-P. Shi, J. Asian Nat. Prod. Res., 2023, 15, 502-506.

167 F. Li, Q. Sun, L. Hong, L. Li, Y. Wu, M. Xia, T. Ikejima, Y. Peng and S. Song, Bioorg. Med. Chem. Lett., 2013, 23, 2500-2504.

168 K. K. Bang, C.-Y. Yun, C. Lee, Q. Jin, J. W. Lee, S.-H. Jung, D. Lee, M. K. Lee, J. T. Hong, Y. Kim and B. Y. Hwang, Bioorg. Med. Chem. Lett., 2013, 23, 3334-3337.

169 X.-D. Wu, L.-C. Zhang, J. He, G.-T. Li, L.-F. Ding, X. Gao, L.-B. Dong, L.-D. Song, Y. Li and Q.-S. Zhao, J. Asian Nat. Prod. Res., 2013, 15, 151-157.

170 S. M. Ghanadian, A. M. Ayatollahi, M. A. Mesaik and O. M. Abdalla, Nat. Prod. Res., 2013, 27, 246-254.

171 H.-B. Wang, L.-P. Liu and X.-Y. Wang, Magn. Reson. Chem., 2013, 51, 580-592.

172 R. K. Devappa, C. C. Malakar, H. P. S. Makkar and K. Becker, Nat. Prod. Res., 2013, 27, 1459-1462.

173 X. Liang, G. Grue-S0rensen, K. Mansson, P. Veds0, A. Soor, M. Stahlhut, M. Bertelsen, K. M. Engell and T. Hogberg, Bioorg. Med. Chem. Lett., 2013, 23, 5624-5629.

174 A. J. Catino, A. Sherlock, P. Shieh, J. S. Wzorek and D. A. Evans, Org. Lett., 2013, 15, 3330-3333.

175 H. Takekawa, K. Tanaka, E. Fukushi, K. Matsuo, T. Nehira and M. Hashimoto, J. Nat. Prod., 2013, 76, 1047-1051.

176 C. Wang, D. Wang and S. Gao, Org. Lett., 2013, 15, 44024405.

177 Y.-G. Wang, J. Ren, A.-G. Wang, J.-B. Yang, T.-F. Li, Q.-G. Ma, J. Tian and Y.-L. Su, J. Nat. Prod., 2013, 76, 2074-2079.

178 J. M. H. Lu, M. V. Perkins and H. J. Griesser, Tetrahedron, 2013, 69, 6468-6473.

179 B. Yang, G.-Y. Chen, X.-P. Song, L.-Q. Yang, C.-R. Han, X.-Y. Wu, C.-J. Zheng, X. Ran and R.-F. Tang, Tetrahedron Lett., 2013, 54, 6434-6436.