A chemoenzymatic approach to the synthesis of enantiomerically pure aza analogues of paraconic acid methyl ester and both enantiomers of methyl β-proline
- 21 December 2001
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 12 (23) , 3241-3249
- https://doi.org/10.1016/s0957-4166(01)00523-7
Abstract
No abstract availableKeywords
This publication has 55 references indexed in Scilit:
- Total Synthesis and Biological Activity of Lactacystin, Omuralide and Analogs.CHEMICAL & PHARMACEUTICAL BULLETIN, 1999
- A Formal Synthesis of (-)-α-Kainic AcidSynlett, 1998
- Enantiodivergent Chemoenzymatic Synthesis of (R)- and (S)-β-Proline in High Optical PurityThe Journal of Organic Chemistry, 1997
- Total synthesis of (±)-methylenolactocin by radical cyclisation of an epoxide using a transition-metal radicalJournal of the Chemical Society, Perkin Transactions 1, 1996
- Synthesis of pyrrolidinones via free-radical cyclisations: potential application to the kainoidsJournal of the Chemical Society, Perkin Transactions 1, 1994
- The synthesis of aracemic 4-substituted pyrrolidinones and 3-substituted pyrrolidines. An asymmetric synthesis of (-)-rolipramThe Journal of Organic Chemistry, 1993
- Preparation of Fused Bis(α-methylene-γ-lactams)Synthesis, 1993
- .beta.-Lactam analogs of oxotremorine. 3- and 4-Methyl-substituted 2-azetidinonesJournal of Medicinal Chemistry, 1990
- Synthesis of tertiary amines by selective diborane reductionThe Journal of Organic Chemistry, 1976
- Borane reduction of amido estersThe Journal of Organic Chemistry, 1968