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Diterpenoid

Synthetic and mechanistic aspects of iatramolecular cycli2ation in the tricycHc diterpenoid area have been studied in detail. In general, the presence of electron withdrawing groups such as carbonyl in the side chain retard the rates of cycli2ation (61). [Pg.555]

The synthesis of cafestol, an antiinflammatory agent which occurs in coffee beans along with related diterpenoids such as actractyloside and kahweol, was accomplished by the same strategic approach which was applied to its companion atractyligenin. [Pg.201]

Kahweol, a "coffee" diterpenoid, was synthesized from the co-occurring natural product cafestol. [Pg.204]

Diisocyanoadociane, a novel marine-derived diterpenoid, was analyzed retrosynthetically using the intramolecular Diels-Alder transform as T-goal concurrently with topological and stereochemical guidance. The enantioselective synthesis outlined below allowed assignment of absolute configuration. [Pg.218]

Heterocycles in synthesis of drimane sesquiterpenoids from labdane diterpenoids 97IZV896. [Pg.222]

Chemistry of taxol, anticancer diterpenoid with oxethane cycle as a part of fused system 98PAC331. [Pg.239]

Furosclerodanes (diterpenoids including furan or y-butyrolactone cycle) from Teucrium genus 9814(48)2185. [Pg.240]

Synthesis of paclitaxel and resiniferatoxin analogs, diterpenoids with oxetane fragments 97G461. [Pg.240]

Total synthesis of taxoids, diterpenoids with 0-heterocyclic fragments 97H(46)727. [Pg.241]

Terpenoids are classified according to the number of five-carbon multiples they contain. Monoterpenoids contain 10 carbons and are derived from two isopentenyl diphosphates, sesquiterpenoids contain 15 carbons and are derived from three isopentenyl diphosphates, diterpenoids contain 20 carbons and are derived from four isopentenyl diphosphates, and so on, up to triterpenoids (C30) and tetraterpenoids (C40). Monoterpenoids and sesquiterpenoids are found primarily in plants, bacteria, and fungi, but the higher terpenoids occur in both plants and animals. The triterpenoid lanosterol, for example, is the precursor from which steroid hormones are made, and the tetraterpenoid /3-carotene is a dietary source of vitamin A (Figure 27.6). [Pg.1071]

The terpenoid precursor isopentenyl diphosphate, formerly called isopentenyl pyrophosphate and abbreviated IPP, is biosynthesized by two different pathways depending on the organism and the structure of the final product. In animals and higher plants, sesquiterpenoids and triterpenoids arise primarily from the mevalonate pathway, whereas monoterpenoids, diterpenoids, and tetraterpenoids are biosynthesized by the 1-deoxyxylulose 5-phosphate (DXP) pathway. In bacteria,... [Pg.1071]

Diterpenoids are derived biosynthetically from geranylgeranyl diphosphate (GGPP), which is itself biosynthesized by reaction of farnesvl diphosphate with isopentenyl diphosphate. Show the structure of GGPP, and propose a mechanism for its biosynthesis horn FPP and IPP. [Pg.1098]

The benzannulation reaction of ethynylferrocene 120 with the diterpenoid chromium alkoxycarbene 119 leads to novel diterpenoid ferrocenyl quinones 121 which, due to their electron-transfer properties, are regarded as potential candidates for non-linear optical materials [71] (Scheme 52). [Pg.149]

Tokoroyama T. Synthesis of Clerodane Diterpenoids and Related Compounds -Stereoselective Construction of the DecaUn Skeleton With Multiple Contiguous Stereogenic Centers Synthesis 2000 611-633... [Pg.301]

Keywords diterpenes, stereoseiective construction of the decaiin skeieton of cierodane diterpenoids... [Pg.301]

Bruno M, Piozzi F, Rosselli S. Natural and hemisynthetic neoclerodane diterpenoids from Scutellaria and their antifeedant activity. Nat Prod Rep 2002 19 357-78. [Pg.119]

Makinoa crispata (Steph.) Miyake from Japan was shown by Hashimoto et al. (1989) to contain diterpene derivatives of the sort illustrated as [466-469] (see Fig. 5.7 for stractures). More recently, Liu and Wu (1997) reported the presence of the rearranged abietane-type diterpenoid derivative makanin [470] from plant material of M. crispata collected on Taiwan. Of note was the apparent absence of any of these compounds in the Japanese plants. [Pg.233]

Leong, Y.-W. and Harrison, L. J. 1997. ent-Trachylobane diterpenoids from the liverwort Mastigophora diclados. Phytochemistry 45 1457-1459. [Pg.319]

Liu, H.-J. and Wu, C.-L. 1997. A rearranged abietane-type diterpenoid from the liverwort Makinoa crispata. Phytochemistry 44 1523-1525. [Pg.320]

Yu Z, GR Stewart, W Mohn (2000) Apparent contradiction psychrotolerant bacteria from hydrocarbon-contaminated arctic tundra soils that degrade diterpenoids synthesized by trees. Appl Environ Microbiol 66 5148-5154. [Pg.91]

Smith DJ, VJJ Martin, WH Mohn (2004) A cytochrome P450 involved in the metabolism of abietane diterpenoids by Pseudomonas abietaniphila BMKE-9. J Bacterial 186 3631-3639. [Pg.145]

Hanson JR, PB Reese, JA Takahashi, MR Wilson (1994) Biotransformation of some stemodane diterpenoids by Cephalosporium aphidicola. Phytochem 36 1391-1393. [Pg.347]

Martin VJJ, WW Mohn (2000) Genetic investigation of the catabolic pathway for degradation of abietane diterpenoids by Pseudomonas abietaniphila BKME-9. J Bacteriol 182 3784-3793. [Pg.348]

Sultankhodzhaev et al. (2005) reported tyrosinase inhibition studies on 15 diterpenoid alkaloids with the lycoctonine skeleton, and their semisynthetic... [Pg.83]

Table 2 Tyrosinase inhibitory activities of the diterpenoid and napelline type alkaloids and their derivatives [49]... Table 2 Tyrosinase inhibitory activities of the diterpenoid and napelline type alkaloids and their derivatives [49]...
Sultankhodzhaev MN et al. (2005) Tyrosinase inhibition studies of diterpenoid alkaloids and their derivatives structure-activity relationships. Nat Prod Res 19(5) 517-522... [Pg.96]


See other pages where Diterpenoid is mentioned: [Pg.9]    [Pg.313]    [Pg.381]    [Pg.430]    [Pg.72]    [Pg.77]    [Pg.727]    [Pg.92]    [Pg.1295]    [Pg.4]    [Pg.326]    [Pg.408]    [Pg.320]    [Pg.65]    [Pg.190]    [Pg.323]    [Pg.344]    [Pg.344]    [Pg.346]    [Pg.75]    [Pg.83]    [Pg.93]   
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Abietane diterpenoids

Aconitum alkaloids diterpenoid

Acyclic diterpenoids

Ageing diterpenoid

Amphilectane-type diterpenoids

Anti-inflammatory diterpenoids

Antimalarial diterpenoids

Baccharis genus diterpenoids from

Baccharis multiflora kaurane-type diterpenoids fro

Bicyclic Diterpenoids

Bioactive diterpenoids

Bioactive diterpenoids cytotoxicity

Biologically active diterpenoids

Briarane diterpenoids

C20-Diterpenoid alkaloid

C2o-diterpenoid alkaloids

Cembrane diterpenoids

Ci9-diterpenoid alkaloids

Clerodane Diterpenoids

Cyathin diterpenoids

Cyclic diterpenoids

Cytotoxic diterpenoid chlorodesmin

Daphnane diterpenoids

Daphnane diterpenoids synthesis

Daphnane diterpenoids via Cope rearrangement

Delphinium alkaloids diterpenoid

Diterpenes Diterpenoids

Diterpenoid DMAPP

Diterpenoid Total Synthesis

Diterpenoid alkaloid aconitine

Diterpenoid alkaloid delphinine

Diterpenoid alkaloid lappaconitine

Diterpenoid alkaloid mesaconitine

Diterpenoid alkaloids

Diterpenoid alkaloids Garrya

Diterpenoid alkaloids chemistry

Diterpenoid alkaloids structure

Diterpenoid alkaloids synthesis

Diterpenoid biosynthesis

Diterpenoid diphosphate

Diterpenoid ginkgolides

Diterpenoid glycosides

Diterpenoid mass spectrometry

Diterpenoid metabolites

Diterpenoid pyrones

Diterpenoid pyrones nalanthalide

Diterpenoid resins

Diterpenoid resins mass spectrometry

Diterpenoid resins spectrometry

Diterpenoid type alkaloids

Diterpenoides

Diterpenoides

Diterpenoids

Diterpenoids Homer-Wadsworth-Emmons reaction

Diterpenoids aphidicolin

Diterpenoids biological activity

Diterpenoids biosynthesis

Diterpenoids bitterness

Diterpenoids chemical conversions

Diterpenoids discovery

Diterpenoids epicandicandiol

Diterpenoids from Aristolochia species

Diterpenoids from Scoparia dulcis

Diterpenoids interconversions

Diterpenoids isolation

Diterpenoids isolinearol

Diterpenoids linearol

Diterpenoids of Rabdosia species

Diterpenoids physiological activity

Diterpenoids properties

Diterpenoids pyrophosphate

Diterpenoids reactions

Diterpenoids rosanes

Diterpenoids sources

Diterpenoids structure determination

Diterpenoids structures

Diterpenoids synthesis

Diterpenoids tetracyclic

Diterpenoids with growth-regulating

Diterpenoids, chemistry

Domino reactions diterpenoids

Edward Leete The Toxicology and Pharmacology of Diterpenoid Alkaloids

Enmein type diterpenoids

Eunicellane diterpenoids

Eunicellin diterpenoids

Euphorbia diterpenoid esters

Fusicoccane diterpenoid

Growth activity, diterpenoids with

Hepaticae diterpenoids

High performance liquid chromatography diterpenoids

Ingenane diterpenoids

Ingenane diterpenoids via Cope rearrangement

Kalihinane diterpenoids

Kaurene-type diterpenoids

Kaurenoid Diterpenoids

Labdane diterpenoids

Labdane-type diterpenoids

Macrocyclic Diterpenoids

Macrocyclic Diterpenoids and their Cyclization Products

Marine diterpenoids

Marine-derived diterpenoid

Miscellaneous Diterpenoids

Neo-Clerodane diterpenoids

New diterpenoid alkaloids

Norlabdane diterpenoids

Of diterpenoids

Of neo-clerodane diterpenoid

Of scopadulane-type diterpenoid

Of tetracyclic diterpenoids

Pimarane-type diterpenoids

Rabdosia Diterpenoids and Their Sources

Rabdosia diterpenoids

Rabdosia diterpenoids classification

Rabdosia diterpenoids from

Rabdosia species diterpenoids from

Rearranged diterpenoids

Rosane diterpenoids

Sacculatane diterpenoids

Scopadulan- type diterpenoid

Scopadulan- type diterpenoids

Scopadulane-type diterpenoids

Sideritis diterpenoids

Spatane diterpenoids

Spirolactone-type diterpenoids

Spongian diterpenoids

Stemodane diterpenoids

Structure activity relationship of scopadulan-type diterpenoid

Syntheses of Diterpenoid Alkaloid Intermediates

Synthesis of Diterpenoids

Synthesis of the Mesotricyclic Diterpenoids Jatrophatrione and

Synthetic Studies directed toward the Diterpenoid Alkaloids

Taxane diterpenoids

Terpenoid resins diterpenoid

Terpenoids diterpenoid resins

Terpenoids diterpenoids

The Diterpenoid Alkaloids from Aconitum, Delphinium, and Garrya Species by E. S. Stern

Tigliane diterpenoids

Tigliane diterpenoids via Cope rearrangement

Tricyclic diterpenoids

Tricyclic diterpenoids synthesis

Vibsane-type diterpenoids

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