HIGHLY SELECTIVE CYCLOTRIMERIZATION OF LITHOCHOLIC ACID BY DCC DMAP REAGENT/

Authors
Citation
Hw. Gao et Jr. Dias, HIGHLY SELECTIVE CYCLOTRIMERIZATION OF LITHOCHOLIC ACID BY DCC DMAP REAGENT/, Croatica chemica acta, 71(3), 1998, pp. 827-831
Citations number
10
Categorie Soggetti
Chemistry
Journal title
ISSN journal
00111643
Volume
71
Issue
3
Year of publication
1998
Pages
827 - 831
Database
ISI
SICI code
0011-1643(1998)71:3<827:HSCOLA>2.0.ZU;2-R
Abstract
Synthesis of cyclolithocholates by using dicyclohexylcarboimide (DCC) and 4-dimethylaminopyridine (DMAP) is described. Cyclotrimerization is the principal reaction route for lithocholic acid system. These react ion conditions were less successful in the cyclization of 12-oxolithoc holic acid.