Complete Diastereocontrol in Intramolecular 1,3-Dipolar Cycloadditions of 2-Substituted 5-Hexenyl and 5-Heptenyl Nitrones: Application to the Synthesis of the β-Lactam Antibiotic 1β-Methylthienamycin-Reference-Cited by-同舟云学术

Complete Diastereocontrol in Intramolecular 1,3-Dipolar Cycloadditions of 2-Substituted 5-Hexenyl and 5-Heptenyl Nitrones: Application to the Synthesis of the β-Lactam Antibiotic 1β-Methylthienamycin

Published:1996-01-01 Issue:13 Volume:61 Page:4427-4433
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Jung Michael E.¹,Vu Binh T.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo952254m

Reference47 articles.

1. American Chemical Society Arthur C. Cope Scholar, 1995.

2. (a) Merck & Co., Inc., U.S. Patent 3 950 357 (April 12, 1976).

3. Structure and absolute configuration of thienamycin

4. Synthetic Carbapenem Antibiotics. I. 1-b-Methylcarbapenem

5. Synthetic carbapenem antibiotics II. Stereoisomers of 7-hydroxyethyl-2,2,5-trimethyl-3-oxa-1-azabicyclo[4.2.O]octan-8-one

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