Enantioselective synthesis of (R)- and (S)-4-[(methoxycarbonyl)-methyl]-2-azetidinones from D-glyceraldehyde acetonide
- 31 December 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (29) , 3009-3012
- https://doi.org/10.1016/s0040-4039(00)88082-x
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- A general approach to -carbapenem antibiotics. Enantioselective synthesis of key intermediates for (+)-PS-5, (+)-PS-6, and (+)-thienamycinTetrahedron Letters, 1983
- Stereocontrolled synthesis of D-pentitols, 2-amino-2-deoxy-D-pentitols and 2-deoxy-D-pentitols from D-glyceraldehyde acetonideJournal of the American Chemical Society, 1982
- Synthesis of (S)- and (R)-4[(methoxycarbonyl)methyl]-2-azetidinone by chemicoenzymic approachJournal of the American Chemical Society, 1981
- Synthetic Studies on Optically Active b-Lactams. Chiral Synthesis of Carbapenam Ring System Starting from L-Aspartic AcidHETEROCYCLES, 1980
- Chiral synthesis of prostaglandins (PGE1) from D-glyceraldehydeJournal of the American Chemical Society, 1977
- Stereospecific total synthesis of prostaglandins E3 and F3.alpha.Journal of the American Chemical Society, 1971