Synthesis of β-Lactones by the Regioselective, Cobalt and Lewis Acid Catalyzed Carbonylation of Simple and Functionalized Epoxides-Reference-Cited by-同舟云学术

Synthesis of β-Lactones by the Regioselective, Cobalt and Lewis Acid Catalyzed Carbonylation of Simple and Functionalized Epoxides

Published:2001-07-19 Issue:16 Volume:66 Page:5424-5426
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lee Jong Tae¹,Thomas P. J.¹,Alper Howard¹

Affiliation:

1. Centre for Catalysis Research and Innovation, Department of Chemistry, University of Ottawa, 10 Marie Curie, Ottawa, Ontario, Canada K1N 6N5, and Corporate R&D, The Dow Chemical Company, Midland, Michigan 48674

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010295e

Reference21 articles.

1. Regiospecific metal-catalyzed ring expansion of aziridines to .beta.-lactams

2. Enantiospecific and stereospecific rhodium(I)-catalyzed carbonylation and ring expansion of aziridines. Asymmetric synthesis of .beta.-lactams and the kinetic resolution of aziridines

3. Palladium-catalyzed transformation of a chiral vinylaziridine to a β-lactam. An enantioselective route to the carbapenem (+)-PS-5

4. Novel synthesis of pyrrolidinones by cobalt carbonyl catalyzed carbonylation of azetidines. A new ring-expansion-carbonylation reaction of 2-vinylazetidines to tetrahydroazepinones

5. Inversion of Stereochemistry in the Co2(CO)8-Catalyzed Carbonylation of Aziridines to β-Lactams. The First Synthesis of Highly Strained trans-Bicyclic β-Lactams

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