The Use of Lewis Acids in Radical Chemistry. Chelation-Controlled Radical Reductions of Substituted α-Bromo-β-alkoxy Esters and Chelation-Controlled Radical Addition Reactions-Reference-Cited by-同舟云学术

The Use of Lewis Acids in Radical Chemistry. Chelation-Controlled Radical Reductions of Substituted α-Bromo-β-alkoxy Esters and Chelation-Controlled Radical Addition Reactions

Published:1998-08-28 Issue:19 Volume:63 Page:6554-6565
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Guindon Yvan¹,Rancourt J.¹

Affiliation:

1. Institut de recherches cliniques de Montréal (IRCM), Bio-organic Chemistry Laboratory, 110 avenue des Pins Ouest, Montréal, Québec, Canada H2W 1R7, Department of Chemistry and Department of Biochemistry, Université de Montréal, C.P. 6128, succursale Centre-ville, Montréal, Québec, Canada H3C 3J7, and Bio-Méga Research Division, Boehringer Ingelheim (Canada) Ltd., 2100 rue Cunard, Laval, Québec, Canada H7S 2G5

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo980636x

Reference77 articles.

1. Acyclic stereochemical control in free-radical reactions

2. Acyclic Diastereofacial Selection in Intermolecular Radical Reactions StericvsElectronic Controls

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