The importance of electrostatic effects in controlling π-facial stereoselectivity in nucleophilic additions to carbonyl compounds: an ab initio MO study of a prototype chelation model-Reference-Cited by-同舟云学术

The importance of electrostatic effects in controlling π-facial stereoselectivity in nucleophilic additions to carbonyl compounds: an ab initio MO study of a prototype chelation model

Published:1991 Issue:5 Volume:0 Page:327-330
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Wong Stephen S.,Paddon-Row Michael N.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910000327

Reference24 articles.

1. Theoretical evidence in support of the Anh–Eisenstein electronic model in controlling π-facial stereoselectivity in nucleophilic additions to carbonyl compounds

2. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones

3. Torsional strain involving partial bonds. The steric course of the reaction between allyl magnesium bromide and 4-t-butyl-cyclohexanone

4. Regio- and stereo-selectivities in some nucleophilic reactions

Cited by 90 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. Radical Cyclization of Ynamides to Nitrogen Heterocycles;Synthesis;2022-06-03

2. Stereoselective synthesis of a 4-⍺-glucoside of valienamine and its X-ray structure in complex with Streptomyces coelicolor GlgE1-V279S;Scientific Reports;2021-06-28

3. Diastereoselectivity in Organic Reactions;Steric and Stereoelectronic Effects in Organic Chemistry;2021

4. Ring-Opening Diarylation of Siloxydifluorocyclopropanes by Ag(I) Catalysis: Stereoselective Construction of 2-Fluoroallylic Scaffold;Organic Letters;2017-12-05

5. Diastereoselectivity in Organic Reactions;Steric and Stereoelectronic Effects in Organic Chemistry;2016