Enantiospecific synthesis and absolute configuration of β-lactam, intermediates from 2-amino-1-phenyl-1,3-propanediols
- 1 January 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (46) , 6707-6710
- https://doi.org/10.1016/s0040-4039(00)97153-3
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Studies on lactams. 81. Enantiospecific synthesis and absolute configuration of substituted .beta.-lactams from D-glyceraldehyde acetonideThe Journal of Organic Chemistry, 1988
- Conversion of Beta-Lactams to Versatile Synthons via Molecular Rearrangement and Lactam CleavageHETEROCYCLES, 1988
- Chiral control of the Staudinger reactionPublished by Walter de Gruyter GmbH ,1987
- An Enantioselective β‐Lactam Synthesis Starting from L‐(S)‐Glyceraldehyde AcetonideHelvetica Chimica Acta, 1983
- Simple Preparation of Azetidino[1,2-d]benzodiazepines.Acta Chemica Scandinavica, 1983
- Studies on lactams. Part 65. N-Unsubstituted .beta.-lactams from .beta.-hydroxy-.alpha.-amino acids. Facile preparation of intermediates for isocephalosporinsThe Journal of Organic Chemistry, 1982
- A highly asymmetric synthesis of the O-2-isocephem class of β-lactam antibioticsCanadian Journal of Chemistry, 1980
- An excellent reagent for the removal of the t-butyldimethylsilyl protecting groupTetrahedron Letters, 1979
- Reactions of dichloroketene with 2-protio- and 2-methyl-.DELTA.2-oxazolinesThe Journal of Organic Chemistry, 1975
- Synthesis and proof of structure of a novel 1,4-benzodiazepineTetrahedron Letters, 1971