Synthesis of (22R, 25R)-2a,3a,26-Trihydroxy-5a-furostan-6-one

被引:0
作者
机构
来源
Synthetic Communications | / 28卷 / 10期
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
[31]   SYNTHESIS AND STRUCTURE OF (22R,24R)-6-BETA-ACETOXY-24-METHYL-5-ALPHA-CHOLESTANE-3-BETA,5-ALPHA,22,24-TETROL [J].
LITVINOVSKAYA, RP ;
BARANOVSKII, AV ;
KHRIPACH, VA ;
OVCHINNIKOV, YE ;
STRUCHKOV, YT .
MENDELEEV COMMUNICATIONS, 1994, (03) :89-90
[32]   SYNTHESIS AND BIOLOGICAL-ACTIVITY OF (22E,25R) AND (22E,25S)-22-DEHYDRO-1-ALPHA,25-DIHYDROXY-26-METHYLVITAMIN D3 [J].
HARA, N ;
EGUCHI, T ;
IKEKAWA, N ;
ISHIZUKA, S ;
SATO, J .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1990, 35 (06) :655-664
[33]   STEREOSELECTIVE SYNTHESIS OF (25R)-26-FLUORO-5-CHOLESTEN-3-BETA,25-DIOL 3-ACETATE FROM METHYL 3-BETA-HYDROXY-5-CHOLENOATE [J].
KABAT, MM .
JOURNAL OF FLUORINE CHEMISTRY, 1991, 53 (02) :249-260
[34]   Rapid hydrolysis of bile acid conjugates using microwaves:: Retention of absolute stereochemistry in the hydrolysis of (25R) 3α,7α,12α-trihydroxy-5β-cholestan-26-oyltaurine [J].
Dayal, B ;
Ertel, NH .
LIPIDS, 1998, 33 (03) :333-338
[35]   Synthesis of (22R,23R,24S)-24-methyl-5α-cholestane-3β,6α,22,23-tetraol, a biosynthetic precursor of brassinolide [J].
Khripach, VA ;
Zhabinskii, VN ;
Pavlovskii, ND .
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2001, 37 (11) :1570-1574
[36]   Synthesis of (22R,23R,24S)-24-Methyl-5α-cholestane-3β,6α,22,23-tetraol, a Biosynthetic Precursor of Brassinolide [J].
V. A. Khripach ;
V. N. Zhabinskii ;
N. D. Pavlovskii .
Russian Journal of Organic Chemistry, 2001, 37 :1570-1574
[37]   Differential behavior of (25R)-5,6-epoxyspirostan-22 alpha-O-3 beta-ol and (25R)-5,6-epoxyspirostan-22 alpha-O-3 beta,4 beta-diol toward Dowex [J].
Korde, SS ;
Baig, MHA ;
Desai, UR ;
Trivedi, GK .
STEROIDS, 1996, 61 (05) :290-295
[38]   Chemical synthesis of the (25R)- and (25S)-epimers of 3α,7α,12α-trihydroxy-5α-cholestan-27-oic acid as well as their corresponding glycine and taurine conjugates [J].
Ogawa, Shoujiro ;
Mitamura, Kuniko ;
Ikegawa, Shigeo ;
Krasowski, Matthew D. ;
Hagey, Lee R. ;
Hofmann, Alan F. ;
Iida, Takashi .
CHEMISTRY AND PHYSICS OF LIPIDS, 2011, 164 (05) :368-377
[39]   Solvent-free synthesis of 6β-phenylamino-cholestan-3β,5α-diol and (25R)-6β-phenylaminospirostan-3β,5α-diol as potential antiproliferative agents [J].
Soto-Castro, Delia ;
Lara Contreras, Roberto Carlos ;
Pina-Canseco, Maria ;
Santillan, Rosa ;
Teresa Hernandez-Huerta, Maria ;
Negron Silva, Guillermo E. ;
Perez-Campos, Eduardo ;
Rincon, Susana .
STEROIDS, 2017, 126 :92-100
[40]   Stereoselective synthesis of (2R, 3S, 22R, 23E)-6, 6-ethylenedioxy-22-hydroxy-2, 3-isopropylidenedioxy-24-methyl-5α-cholest-23-ene:: An intermediate for the synthesis of castasterone, dolichosterone and brassinolide [J].
Hazra, BG ;
Kumar, TP ;
Pore, VS .
INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 2005, 44 (03) :611-614