The asymmetric synthesis of β-lactam antibiotics-v. Application of chiral α,β-epoxyimines in ketene-imine cycloaddition reactions leading to homochiral 3-aminoazetidinones.-Reference-Cited by-同舟云学术

The asymmetric synthesis of β-lactam antibiotics-v. Application of chiral α,β-epoxyimines in ketene-imine cycloaddition reactions leading to homochiral 3-aminoazetidinones.

Published:1988-01 Issue:40 Volume:29 Page:5065-5068
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Evans David A.,Williams J.Michael

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. The asymmetric synthesis of β-lactam antibiotics - I. application of chiral oxazolidones in the staudinger reaction.

2. The asymmetric synthesis of β-lactam antibiotics -II. The first enantioselective synthesis of the carbacephalosporin nucleus.

3. Nuclear analogs of .beta.-lactam antibiotics. 1. The total synthesis of a 7-oxo-1,3-diazabicyclo[3.2.0]heptane-2-carboxylic acid via a versatile monocyclic .beta.-lactam intermediate

4. Nuclear analogs of .beta.-lactam antibiotics. 2. The total synthesis of 8-oxo-4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acids

5. The Synthesis of (6R*, 7R*)-4-Carboxy-3-hydroxy-7-phenylacetamido-2-isooxacephem

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