Consideration of molecular arrangements in regio- and enantioselective reduction of an NAD model compound controlled by carbonyl oxygen orientation-Reference-Cited by-同舟云学术

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Consideration of molecular arrangements in regio- and enantioselective reduction of an NAD model compound controlled by carbonyl oxygen orientation

Published:2007 Issue:23 Volume:5 Page:3834
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Mikata Yuji,Aida Shiho,Inaba Yoko,Yano Shigenobu

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2007/OB/B710780C

Reference43 articles.

1. NADH mimics for the stereoselective reduction of benzoylformates to the corresponding mandelates.

2. Stereoselectivity of hydrogen transfer with chiral NADH models as a function of configuration and conformation

3. Variations of the nature of the chiral auxiliary with a highly enantioselective chiral NADH model

4. An approach to features responsible for the obtention of high e.e. with a highly enantioselective NADH model

5. Rational design of novel axially chiral NADH models based on configurational control of atropisomeric lactams

Cited by 1 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. Oxidation and Reduction;Organic Reaction Mechanisms Series;2011-08-05

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