Simple and condensed β-lactams. Part 29. Synthesis and base-catalyzed ring transformation of 4-[(2RS,3SR)-3-hydroxy-1-(4-methoxyphenyl)-4-oxoazetidin-2-yl)]thiazol-2(3H)-one-Reference-Cited by-同舟云学术

Simple and condensed β-lactams. Part 29. Synthesis and base-catalyzed ring transformation of 4-[(2RS,3SR)-3-hydroxy-1-(4-methoxyphenyl)-4-oxoazetidin-2-yl)]thiazol-2(3H)-one

Published:1997-09 Issue:37 Volume:53 Page:12729-12738
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Sápi Attila,Fetter József,Lempert Károly,Kajtár-Peredy Mária,Czira Gábor

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference7 articles.

1. Simple and condensed β-lactams. Part 22. An unprecedented ring transformation accompanying dephthaloylation of a 3-phthalimidoazetidin-2-one

2. Studies on lactams—VII

3. Novel and effective routes to optically pure amino acids, dipeptides, and their derivatives viaβ-lactams obtained through asymmetric cycloaddition

4. New reactivity patterns of the .beta.-lactam ring: tandem C3-C4 bond breakage-rearrangement of 4-acyl- or 4-imino-3,3-dimethoxy-2-azetidinones promoted by stannous chloride (SnCl2-2H2O)

5. From Penicillins to 4,5-Dioxothiazolidines: A Thermal Rearrangement of Tritylaminopenam Derivatives

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