Simple and condensed β-lactams. Part 22. An unprecedented ring transformation accompanying dephthaloylation of a 3-phthalimidoazetidin-2-one
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. An Unprecedented Cleavage of the .beta.-Lactam Ring: Stereoselective Synthesis of Chiral .beta.-Amido Cyanides
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. From Penicillins to 4,5-Dioxothiazolidines: A Thermal Rearrangement of Tritylaminopenam Derivatives
5. Contrasting thermal behaviour of diastereoisomeric 4-acetylthio-3-acylamino-1-(α-triphenylphosphoranylidene)alkoxycarbonylmethylazetidin-2-ones
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3. Synthesis of 1,4-Diazabutadienes (=N,N′-Ethane-1,2-diylidenebis[amines]) by Grinding;Helvetica Chimica Acta;2011-01
4. ChemInform Abstract: Simple and Condensed β-Lactams. Part 22. An Unprecedented Ring Transformation Accompanying Dephthaloylation of a 3- Phthalimidoazetidin-2-one.;ChemInform;2010-08-17
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