β-Lactam synthesis: Chemospecific sulfonation and cyclization of the β-hydroxyvaline nucleus-Reference-Cited by-同舟云学术

β-Lactam synthesis: Chemospecific sulfonation and cyclization of the β-hydroxyvaline nucleus

Published:1986-01 Issue:25 Volume:27 Page:2789-2792
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Slusarchyk W.A,Dejneka T,Gougoutas J,Koster W.H,Kronenthal D.R,Malley M,Perri M.G,Routh F.L,Sundeen J.E,Weaver E.R,Zahler R,Godfrey J.D,Mueller R.H,Von Langen D.J

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. O-Sulfated .beta.-lactam hydroxamic acids (monosulfactams). Novel monocyclic .beta.-lactam antibiotics of synthetic origin

2. Monobactams: Ring Activating N-1-Substituents in Monocyclic b-Lactam Antibiotics

3. F. G. Pilkiewicz, unpublished results.

4. J. Antimicrob. Chemother.;Aztreonam, a Synthetic Monobactam,1981

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