An amidyl radical cyclisation approach towards the synthesis of β-lactams
- 1 March 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (10) , 1265-1268
- https://doi.org/10.1016/s0040-4039(97)10772-9
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Iminyl Radicals: A Fresh Look at a Forgotten Species (and Some of its Relatives)Synlett, 1996
- Radical Cyclization Approach to 4-Oxo-2-azetidineacetic Acids: Synthesis of a Chiral Key Intermediate for Carbapenem Antibiotic PS-5Synlett, 1995
- Iminyl, amidyl, and carbamyl radicals from O-benzoyl oximes and O-benzoyl hydroxamic acid derivativesTetrahedron, 1995
- Sulfur-Directed Regioselective Radical Cyclization Leading to .beta.-Lactams: Formal Synthesis of (.+-.)-PS-5 and (+)-ThienamycinThe Journal of Organic Chemistry, 1995
- Asymmetric Induction in Radical Cyclization Leading to β-Lactams: Formal Synthesis of (+)-PS-5Synlett, 1994
- Amidyl radicals from N-(phenylthio)amidesTetrahedron Letters, 1993
- The Generation of Nitrogen Radicals and Their Cyclizations for the Construction of the Pyrrolidine NucleusPublished by Elsevier ,1993
- Synthesis of β-Lactams by Means of Sulfur-Controlled Regioselective Radical Cyclizations ofN-Ethenyl-α-bromoalkanamidesSynlett, 1993
- The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 2Synthesis, 1988
- The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 1Synthesis, 1988