Carbonyl Orientation Determines Regio- and Enantioselectivity in 1,2-/1,4-Reduction of an NAD Model Compound-Reference-Cited by-同舟云学术

Carbonyl Orientation Determines Regio- and Enantioselectivity in 1,2-/1,4-Reduction of an NAD Model Compound

Published:2004-07-23 Issue:17 Volume:6 Page:2921-2924
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Mikata Yuji¹,Aida Shiho¹,Yano Shigenobu¹

Affiliation:

1. KYOUSEI Science Center, Nara Women’s University, Nara 630-8506, Japan, and Division of Material Science, Graduate School of Humanities and Sciences, Nara Women's University, Nara 630-8506, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol048983i

Reference25 articles.

1. Burgess, V. A.; Davies, S. G.; Skerlj, R. T.Tetrahedron: Asymmetry1991,2, 299.

2. Nad(P)+-nad(p)h models. 57

3. NAD(P)+-NAD(P)H models. 66. Stereospecific interconversion between different chiralities in the reduction of a quinolinium salt

4. NAD(P)+–NAD(P)H Models. 87. Nonsteric Stereochemistry Controlled by a Carbonyl Dipole

5. NAD(P)+–NAD(P)H Models. 86. Nonsteric Stereochemistry in Hydride-Transfer to Sulfinylpyridinium Ion

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