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The azomethine ylid strategy for β‐lactam synthesis
Author(s) -
Gallagher Timothy
Publication year - 1999
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570360602
Subject(s) - chemistry , lactam , heteroatom , bicyclic molecule , combinatorial chemistry , scope (computer science) , stereochemistry , organic chemistry , ring (chemistry) , computer science , programming language
Abstract A summary of the development, mechanistic features, and scope of the azomethine ylid strategy for the synthesis of a variety of bicyclic β‐lactam derivatives, including carbapenams, carbapenems as well as heteroatom substituted variants, is presented.