Modulation of cholesterol esterase's diastereoselectivity by chiral auxiliaries. The very large effect of a dihydroxy bile salt on the hydrolysis of .alpha.-tocopheryl acetates-Reference-Cited by-同舟云学术

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Modulation of cholesterol esterase's diastereoselectivity by chiral auxiliaries. The very large effect of a dihydroxy bile salt on the hydrolysis of .alpha.-tocopheryl acetates

Published:1994-07 Issue:15 Volume:116 Page:6945-6946
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Moore A.,Burton G. W.,Ingold K. U.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00094a063

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Nutrients central to maintaining intestinal absorptive efficiency and barrier integrity with fowl;Poultry Science;2017-05

2. α‐Tocopherol Stereoisomers;Vitamin E;2007

3. Hydrolysis of tocopheryl and retinyl esters by porcine carboxyl ester hydrolase is affected by their carboxylate moiety and bile acids;The Journal of Nutritional Biochemistry;2001-04

4. Design and synthesis of analogs of vitamin E: Antiproliferative activity against human breast adenocarcinoma cells;Bioorganic & Medicinal Chemistry Letters;1998-09

5. Kinetic resolution of sulfoxides with pendant acetoxy groups using cholesterol esterase: substrate mapping and an empirical rule for chiral phenols;Canadian Journal of Chemistry;1995-08-01

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