Literature DB >> 1790581

The use of microwave oven for the rapid hydrolysis of bile acid methyl esters.

B Dayal1, G Salen, V Dayal.   

Abstract

An efficient and convenient procedure for the hydrolysis of bile acid methyl esters is described. This is achieved by the addition of aqueous lithium hydroxide in methanol/dioxane/tetrahydrofuran (or dimethylformamide) in the microwave oven. Under these conditions the formates as well as the acetate derivatives prepared under microwave irradiation conditions were also hydrolyzed, and the desired bile acids were isolated in 86-94% yield. All these reactions were completed in the microwave oven within 45-60 s.

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Year:  1991        PMID: 1790581     DOI: 10.1016/0009-3084(91)90068-m

Source DB:  PubMed          Journal:  Chem Phys Lipids        ISSN: 0009-3084            Impact factor:   3.329


  3 in total

1.  Rapid hydrolysis of bile acid conjugates using microwaves: retention of absolute stereochemistry in the hydrolysis of (25R) 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestan-26-oyltaurine.

Authors:  B Dayal; N H Ertel
Journal:  Lipids       Date:  1998-03       Impact factor: 1.880

2.  Studies on N-nitroso bile acid amides in relation to their possible role in gastrointestinal cancer.

Authors:  B Dayal; N H Ertel
Journal:  Lipids       Date:  1997-12       Impact factor: 1.880

Review 3.  Chemical and metabolic transformations of selected bile acids.

Authors:  K Kuhajda; S Kevresan; J Kandrac; J P Fawcett; M Mikov
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2006 Jul-Sep       Impact factor: 2.441

  3 in total

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