β-Lactam-Based Azomethine Ylide Reactivity. Expedient Synthesis of Carbapenams and Carbapenems-Reference-Cited by-同舟云学术

β-Lactam-Based Azomethine Ylide Reactivity. Expedient Synthesis of Carbapenams and Carbapenems

Published:1997-03-01 Issue:9 Volume:119 Page:2309-2310
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Martel Sarah R.¹,Wisedale Richard¹,Gallagher Timothy¹,Hall Lee D.¹,Mahon Mary F.¹,Bradbury Robert H.¹,Hales Neil J.¹

Affiliation:

1. School of Chemistry, University of Bristol Bristol BS8 1TS, U.K. X-ray Crystallographic Unit, School of Chemistry University of Bristol, Bristol, BS8 1TS, U.K. X-ray Crystallographic Unit, School of Chemistry University of Bath, Bath, BA2 7AY, U.K. Zeneca Pharmaceuticals, Mereside, Alderley Park Macclesfield SK10 4TG, U.K.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9637560

Reference19 articles.

1. Recent Developments in the Field of β-Lactam Antibiotics

2. (a) Lown, J. W. In1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; Wiley: New York, 1984; Vol. 1, p 653.

3. Prototropic routes to 1,3- and 1,5-dipoles, and 1,2-ylides: applications to the synthesis of heterocyclic compounds

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