Potential bile acid metabolites. 25. Synthesis and chemical properties of stereoisomeric 3alpha,7alpha,16- and 3alpha,7alpha,15-trihydroxy-5beta-cholan-24-oic acids. 2002

Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
College of Humanities and Sciences, Nihon University, Japan. takaiida@chs.nihon-u.ac.jp

Epimeric 3alpha,7alpha,16- and 3alpha,7alpha,15-trihydroxy-5beta-cholan-24-oic acids and some related compounds were synthesized from chenodeoxycholic acid (CDCA) and ursodeoxycholic acid (UDCA), respectively. The key reaction involved one-step remote oxyfunctionalization of unactivated methine carbons at C-17 of CDCA and at C-14 of UDCA as their methyl ester-peracetate derivatives with dimethyldioxirane (DMDO). After dehydration of the resulting 17alpha- and 14alpha-hydroxy derivatives with POCl(3) or conc. H(2)SO(4), the respective Delta(16)- and Delta(14)-unsaturated products were subjected to hydration via hydroboration followed by oxidation to yield the 3,7,16- and 3,7,15-triketones, respectively. Stereoselective reduction of the respective triketones with tert-butylamine-borane complex afforded the epimeric 3alpha,7alpha,16- or 3alpha,7alpha,15-trihydroxy derivatives exclusively. A facile formation of the corresponding epsilon-lactones between the side chain carboxyl group at C-24 and the 16alpha- (or 16beta-) hydroxyl group in bile acids is also clarified.

UI MeSH Term Description Entries
D002635 Chenodeoxycholic Acid A bile acid, usually conjugated with either glycine or taurine. It acts as a detergent to solubilize fats for intestinal absorption and is reabsorbed by the small intestine. It is used as cholagogue, a choleretic laxative, and to prevent or dissolve gallstones. Chenic Acid,Chenodeoxycholate,Chenodiol,Gallodesoxycholic Acid,Chenique Acid,Chenix,Chenofalk,Chenophalk,Henohol,Quenobilan,Quenocol,Sodium Chenodeoxycholate,Acid, Chenic,Acid, Chenique,Acid, Chenodeoxycholic,Acid, Gallodesoxycholic,Chenodeoxycholate, Sodium
D001647 Bile Acids and Salts Steroid acids and salts. The primary bile acids are derived from cholesterol in the liver and usually conjugated with glycine or taurine. The secondary bile acids are further modified by bacteria in the intestine. They play an important role in the digestion and absorption of fat. They have also been used pharmacologically, especially in the treatment of gallstones. Bile Acid,Bile Salt,Bile Salts,Bile Acids,Acid, Bile,Acids, Bile,Salt, Bile,Salts, Bile
D013237 Stereoisomerism The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed) Molecular Stereochemistry,Stereoisomers,Stereochemistry, Molecular,Stereoisomer

Related Publications

Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
March 2004, Chemical & pharmaceutical bulletin,
Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
July 2006, Journal of lipid research,
Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
March 1975, Steroids,
Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
June 2001, Steroids,
Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
July 1974, Steroids,
Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
January 1976, Journal of lipid research,
Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
December 1978, Steroids,
Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
June 1978, Steroids,
Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
April 1991, Journal of lipid research,
Takashi Iida, and Masahiro Hikosaka, and Genta Kakiyama, and Keisuke Shiraishi, and Claudio D Schteingart, and Lee R Hagey, and Huong-Thu Ton-Nu, and Alan F Hofmann, and Nariyasu Mano, and Junichi Goto, and Toshio Nambara
October 1975, The Journal of biological chemistry,
Copied contents to your clipboard!