Efficient Entry to Highly Functionalized β-Lactams by Regio- and Stereoselective 1,3-Dipolar Cycloaddition Reaction of 2-Azetidinone-Tethered Nitrones. Synthetic Applications-Reference-Cited by-同舟云学术

Efficient Entry to Highly Functionalized β-Lactams by Regio- and Stereoselective 1,3-Dipolar Cycloaddition Reaction of 2-Azetidinone-Tethered Nitrones. Synthetic Applications

Published:2002-09-07 Issue:20 Volume:67 Page:7004-7013
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Alcaide Benito¹,Almendros Pedro¹,Alonso Jose M.¹,Aly Moustafa F.¹,Pardo Carmen¹,Sáez Elena¹,Torres M. Rosario¹

Affiliation:

1. Departamento de Química Orgánica I, Facultad de Química, Universidad Complutense, 28040-Madrid, Spain, and Laboratorio de Difracción de Rayos X, Facultad de Química, Universidad Complutense 28040-Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo025924e

Reference32 articles.

1. The mechanisms of reactions of .beta.-lactam antibiotics

2. Sugar-substituted 2-azetidinone cholesterol absorption inhibitors: Enhanced potency by modification of the sugar

3. Sugar-substituted 2-azetidinones as cholesterol absorption inhibitors

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