## ABSTRAm A facile and regiocontrolled procedure for the preparation of S~-cholestane-3a,7c,l2~,25-tetrol-3-O-fi-o-glucuronide and its corresponding C-26 analogue is described. The method involves direct coupling of bile alcohols, namely, 5/3-cholestane-3rY,7~,12a,25-tetrol and 24-nor-Sp-cholesta
✦ LIBER ✦
New bile alcohols, 5α- and 5β-dermophols from amphibians
✍ Scribed by Kenji Kihira; Misao Yasuhara; Taiju Kuramoto; Takahiko Hoshita
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 206 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Bile alcohol glucuronides: regioselectiv
✍
Bishambar Dayal; Gerald Salen; Janak Padia; Sarah Shefer; George S. Tint; Gino S
📂
Article
📅
1993
🏛
Elsevier Science
🌐
English
⚖ 746 KB
Isolation of 5α- and 5β-dihydrorubroster
✍
M. Báthori; J.-P. Girault; I. Máthé; R. Lafont
📂
Article
📅
2000
🏛
John Wiley and Sons
🌐
English
⚖ 50 KB
ChemInform Abstract: A New Chiral Synthe
✍
D. W. HARNEY; T. A. MACRIDES
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 32 KB
👁 1 views
Bile acids. LXXI. A new synthesis of (25
Bile acids. LXXI. A new synthesis of (25R)-3α, 7α-dihydroxy-[5α,6α-3H2]-5α-cholestan-26-oic acid (1)
✍
Daniel M. Tal (2); William H. Elliott; Edward A. Doisy
📂
Article
📅
1985
🏛
John Wiley and Sons
🌐
French
⚖ 313 KB
## Abstract Tritiation of 7‐oxo‐5‐cholestene‐3β,26‐diol diacetate afforded a mixture of [5α,6α‐^3^H~2~] products which were reduced with lithium aluminum hydride to provide a mixture of [5α,6α‐^3^H~2~]‐3β, (7α and 7β), 26‐triols an 3β, 26‐diol. Oxidation with Jones reagent provided 3,7‐dioxo and 3‐
Transformation of lithocholic acid to a
✍
Songsri Kulprecha; Takuya Nihira; Kazufumi Yamada; Toshiomi Yoshida; Naline Nilu
📂
Article
📅
1985
🏛
Springer
🌐
English
⚖ 574 KB
New 5-Alkoxypyrimidine Derivatives from
✍
Tilman Lechel; Hans-Ulrich Reissig
📂
Article
📅
2010
🏛
John Wiley and Sons
🌐
English
⚖ 652 KB