Orbital-Controlled Stereoselections in Sterically Unbiased Cyclic Systems-Reference-Cited by-同舟云学术

Orbital-Controlled Stereoselections in Sterically Unbiased Cyclic Systems

Published:1999-04-28 Issue:5 Volume:99 Page:1337-1376
ISSN:0009-2665
Container-title:Chemical Reviews
language:en
Short-container-title:Chem. Rev.

Author:

Ohwada Tomohiko¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Nagoya City University, Tanabe-dori, Mizuho-ku, Nagoya, 467, Japan, and Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113, Japan

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cr980371m

Reference232 articles.

1. Role of Frontier Orbitals in Chemical Reactions

2. Theory of Orientation and Stereoselection

3. Crystal structure of the complex 5-phenyladamantan-2-one.antimony pentachloride. Hyperconjugative effects in an activated ketone

4. The twist angle approach to the stereoselectivity in reduction of ketones

5. Geometric equivalents of enantiomers in studies of the stereochemical course of substitution at carbon. Electronic effects in nucleophilic addition to carbonyl groups and to carbocations. Virtual proof of the existence of .sigma. participation by unstrained carbon-carbon bonds

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