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1.
Evidence for the presence of 3β,6α-dihydroxy-5α-chol-9(11)-en-23-one in the aglycone mixture from the starfish Marthasterias glacialis is provided by the synthesis of 3β,6α-dihydroxy-5α-cholan-23-one (19) and its identification in the hydrogenated aglycone mixture. The side-chain is constructed from the 23,24-dinorcholanol (13) by reaction of the 22-tosylate (16) with the acetylide anion, followed by hydration of the resulting 23-yne (17). 相似文献
2.
Cholesterol (1) is used to synthesize again 5-hydroxy-2,7-dien-6-one (5) through the intermediates 2-4. cis-Hydroxylation of 5 with OsO
4
and subsequent acetylation give steroids 6-8. Dehydration of 5-hydroxy-6-ketone 6 forms the unsaturated compounds 9-11 相似文献
3.
《Tetrahedron letters》1986,27(20):2215-2218
4.
An ecdysteroid analog has been synthesized from -sitosterol.Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus', 220141, Belarus', Minsk, ul. Akad. Kuprevich, 5/2. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 488–491, July–August, 1999. 相似文献
5.
Chen ZHANG Guo Jun ZHEN Jin Chun CHEN Li Jing FANG Yu Lin LI 《中国化学快报》2006,17(10):1290-1292
Eudesmane and agarofuran are naturally occurring sesquiterpenoids with characteristic decalin skeletons. These natural products frequently contain multiple hydroxyl groups and contiguous stereocenters. Members from these families show cytotoxic, immuno- s… 相似文献
6.
Martín A. Iglesias Arteaga Roxana Pérez Gil Vivian Leliebre Lara Carlos S. Pérez Martinez Francisco Coll Manchado Arístides Rosado Pérez 《合成通讯》2013,43(8):1381-1386
The synthesis of a plant growth promoter furostanol which bears the characteristic functionality of teasterone on rings A and B is described. 相似文献
7.
《中国化学快报》1997,(9)
Thephotocycloadditionofmethyl2,4-dioxopentanoate1toalkenesorconjugatedolefins2regioselectivelygavethecycloadduct3(Schemel).ThisreactioncouldconvenientlybeusedtoconstructthebasicframeworkofvariousnatUraIlyoccutringchamigran-tyPespirosesquiterPenes,suchasa-chamigrene",6-chamigrene:=,andaseriesofrelatedhaIogenatedderivativesd.The(i)-Q-Chamigrene-3-onewasanewmemberofthisfamilyandwasrecentlyisolatedfromMarchantiapolymorPha".whichpossessedthestrUctUreofasyntheticintermediate,1-methoxycarbonyl-5,… 相似文献
8.
Pregnenolone (2) is used in a novel synthesis of 2,3,20-triacetoxy-6-ketosteroid (6), a key intermediate in the preparation of 20-hydroxyecdysone (1) 相似文献
9.
The reaction of pregnenolone and 3,5-cyclo-5-pregnan-6-ol-20-one with trifluoroperacetic acid produces the trifluoroacetates, hydrolysis of which gives the 3,5alpha;,6-triol. 相似文献
10.
Sesquiterpenesconstituteagroupofnaturalcompoundswhichexhibitconsiderablebiologicalactivities,suchasantiinflamatoryicytyotoxic'andcytotoxic',seedgendnation'andmolluscacidalactivities4.InrecentyearsanumberofC-6oxyfunctionalizedeudesmanesand6-dihydroagarofurans,suchascomPounds3-6',havebeenisolatedfromnaturesources.HoweverthereportSonthesynthesisofthisparticularkindofcompoundsarefewandthereportedsynthesesaregenerallybysyntheticmethodologystartingfroma-santonin2e.Ourinterestofstudyonthesynthesisof… 相似文献
11.
YunFengCHENG YongZhouHU 《中国化学快报》2004,15(11):1281-1284
Herein we reported a one-pot synthesis of arylsubstituted imidazolin-2-ones by thecyclization of ct-aminoacetophenone hydrochloride analogues 2 with arylisocyanates 3. Comparedwith other known synthetic route, this method resulted in higher yield. 相似文献
12.
R. P. Litvinovskaya S. V. Drach V. A. Khripach 《Russian Journal of Organic Chemistry》2001,37(7):952-956
A procedure was developed for preparation of compounds of the cholestane and 26,27-dinorcholestane series with 16-acetoxy-substited ring D and functionalized side chain, starting from 16,17-epoxypregnenolone. 相似文献
13.
Reduction of 17-hydroxyprogesterone (1) with NaBH
4
produces 17,20-dihydroxypregn-4-en-3-one (2) and pregn-4-en-3,17,20-triol (3) 相似文献
14.
Gang ZHOU Xiao Lei GAO Yu Kun GUAN Wei Dong LI Yu Lin LI* National Laboratory of Applied Organic Chemistry Institute of Organic Chemistry Lanzhou University Lanzhou 《中国化学快报》2001,(5)
Sesquiterpenic compounds of the Eudesmane family have attracted considerable attention due to their intriguing biological properties1,2, particularly significant antifeedant activity, cell growth inhibitory and plant growth regulating activities.In 1996, J. Hu and co-workers3 had isolated eudesmane sesquiterpene 5?-hydroxy-isopterocarpolone 1 from the aerial parts of chinese folk medicine Artemisia eriopoda and elucidated its structure by spectropic methods. Herein, we reported the first tota… 相似文献
15.
N. V. Kovganko Yu. G. Chernov S. N. Sokolov Zh. N. Kashkan V. L. Survilo 《Chemistry of Natural Compounds》2009,45(2):200-204
New esters of 3β,5α,6β-trihydroxysteroids and 3β,5-dihydroxy-6-ketosteroids containing 6-chloropyridine groups characteristic
of the alkaloid epibatidine were synthesized by acylation with 6-chloronicotinoylchloride.
Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 175-179, March-April, 2009. 相似文献
17.
Eudesmane derivatives have been drawing considerable attention due to their wide spectrum of biological proerties, particulaly antifeedant, cell growth inhibitory and plant growth regulating activities.1 In recent years a number of C-6 oxyfunctionalized eudesmanes and β-dihydroagarofurans,such as compounds 3-6,have been isolated from nature sources. However the reports on the synthesis of this particular kind of compounds are few and the reported syntheses are generally by synthetic methodology starting from α-santonin 22. Our interest of study on the synthesis of this kind of compounds prompted us to investigate a new synthetic route from cheap material (+)-dihydrocarvone 7. 相似文献
18.
1-Substituted 4-benzylidene-2-{-[3,5-di(tert-butyl)-4-hydroxyphenyl]vinyl}-4-benzylidene-2-imidazolin-5-ones have been synthesized by the interaction of azomethines and N-acylhydrazones (derivatives of 3,5-di(tert-butyl)-4-hydroxybenzaldehyde) with 4-benzylidene-2-methyloxazol-5-one. The acylation of 1,2-bis[3,5-di(tert-butyl)-4-hydroxybenzylideneamino]ethane with acid chlorides in acetonitrile in the presence of triethylamine leads to 1,3-diacyl-2-[3,5-di(tert-butyl)-4-hydroxyphenyl]imidazolidine. 相似文献
19.
-Sitosterol 1 and the intermediate 5-hydroxy-6-ketosteroids 2 and 3 were used to synthesize 5-hydroxy-6-ketosteroid oximes 4 and 5. Dehydration of 5 fromCinachyrellasponges forms (24R,6E)-24-ethylcholest-6-hydroximino-4-en-3-one 6, a steroidal oxime 相似文献
20.
The newderivative 5-chloro-4-methoxysantonin oximewasprepared from5-chloro-4-methoxysantonin by reaction with hydroxylamine hydrochloride in the presence of pyridine. The structure was established by IR, UV, and PMR spectroscopies. 相似文献