Trans diastereoselective synthesis of 3-alkyl substituted β-lactams via the acid chloride-imine reaction of nonactivated acid chlorides-Reference-Cited by-同舟云学术

Trans diastereoselective synthesis of 3-alkyl substituted β-lactams via the acid chloride-imine reaction of nonactivated acid chlorides

Published:1995-04 Issue:15 Volume:36 Page:2555-2558
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Browne Margaret,Burnett Duane A.,Caplen Mary Ann,Chen Lian-Yong,Clader John W.,Domalski Martin,Dugar Sundeep,Pushpavanam Pradeep,Sher Rosy,Vaccaro Wayne,Viziano Monica,Zhao Hongrong

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. 2-Azetidinones as Inhibitors of Cholesterol Absorption

2. The ester enolate-imine condensation route to .beta.-lactams

3. β-Lactam formation by ultrasound-promoted reformatsky type reaction

4. The Organic Chemistry of β-Lactams,1992

5. Alkyl(phenylthio)ketenes as synthetic equivalents of monoalkylketenes: A concise general route to 3-alkyl β-lactams as carbapenem building-blocks

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