β-Lactams from ester enolates and N-TMSimines: Enantioselective synthesis of (6R, 7S)-1β-3-dimethyl-3-isocephem
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. ChemInform Abstract: β-Lactams from Ester Enolates and N-Tms-imines: Enantioselective Synthesis of (6R,7S)-1β-3-Dimethyl-3-isocephem.;ChemInform;2010-08-17
2. A Simple Method for Deprotection of the N- and O-Carbobenzoxy Groups and N-Methylation of the Desosamine Sugar Moiety of Ketolides;The Journal of Antibiotics;2005-11
3. Recent synthetic applications of the non-classical Wittig reaction;Journal of the Chemical Society, Perkin Transactions 1;1999
4. Trans -Diastereoselective synthesis of 3-phthalimido β-lactams via a two step-staudinger reaction;Tetrahedron Letters;1996-06
5. Efficient synthesis of the four diastereomers of phosphothreonine from lactalhehyde;Tetrahedron: Asymmetry;1996-05
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