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Transformation of lithocholic acid to a new bile acid, 3α, 15β-dihydroxy-5β-cholanic acid byCunninghamella blakesleeanaST-22

✍ Scribed by Songsri Kulprecha; Takuya Nihira; Kazufumi Yamada; Toshiomi Yoshida; Naline Nilubol; Hisaharu Taguchi


Publisher
Springer
Year
1985
Tongue
English
Weight
574 KB
Volume
22
Category
Article
ISSN
1432-0614

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13C NMR spectral assignments of 3α,3′α-b
✍ Jari Tamminen; Kari Lappalainen; Katri Laihia; Pia Mänttäri; Hannu Salo; Erkki K 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 101 KB

3a,3@a-Bis(arylcarboxy)-5b-cholan-24-oic acid ethane-1, 2-diol diesters (1È3) were synthesized by the reaction of an aroyl chloride (aroyl \ 2,6-dichlorobenzoyl, 2-naphthoyl and 1-pyrenoyl) with lithocholic acid (3a-hydroxy-5b-cholan-24-oic acid) ethane-1,2-diol diester. The 13C NMR chemical shift a