d-Glucosamine propanedithioacetal, an efficient chiral auxiliary in β-Lactam chemistry1Dedicated to Professor Sir Derek H. R. Barton.1
- 28 May 1999
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 7 (5) , 837-850
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Different approaches to the asymmetric synthesis of 1,3,6-trisubstituted and 1,2,3,6-tetrasubstituted carbapenems1 from D-glucosamineTetrahedron: Asymmetry, 1995
- The use of radical decarboxylation in the preparation of 1-methylcarbapenem antibiotic precursors from D-glucosamineTetrahedron: Asymmetry, 1994
- Three 1,3,4-trisubstituted β-lactam antibioticsActa Crystallographica Section C Crystal Structure Communications, 1994
- Enantioselective synthesis and antielastase activity of 1,3,4-trisubstituted and 3,4-disubstituted β-lactam antibioticsBioorganic & Medicinal Chemistry Letters, 1993
- The Use of Radical Cyclization in the Preparation of Substituted Methyl Carbapenem Antibiotic PrecursorsAngewandte Chemie International Edition, 1993
- Enantioselective synthesis of 2-isocephem and 2-oxa-isocephem antibioticsTetrahedron Letters, 1992
- Monocyclic β-lactam inhibitors of human leukocyte elastaseTetrahedron, 1990
- Asymmetric synthesis of 1,3,4-trisubstituted and 3,4-disubstituted 2-azetidinones: strategy based on use of D -glucosamine as a chiral auxiliary in the Staudinger reactionJournal of the Chemical Society, Perkin Transactions 1, 1990
- Lactam. III. Conformation of (-)-menthone lactam and N-methylmenthone lactamJournal of the American Chemical Society, 1973
- Symmetry rules for optical rotationAccounts of Chemical Research, 1968