Creation of Novel Chiral Synthons with Pig Liver Esterase: Application to Natural Product Synthesis and the Substrate Recognition
- 1 January 1986
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Creation of novel chiral synthons with enzymes and applications to natural product synthesis. 15. Efficient introduction of chiral centers into cyclohexane ringTetrahedron Letters, 1984
- A general approach to -carbapenem antibiotics. Enantioselective synthesis of key intermediates for (+)-PS-5, (+)-PS-6, and (+)-thienamycinTetrahedron Letters, 1983
- Stereocontrolled synthesis of an ene-carbapenem antibiotic (-)-asparenomycin CJournal of the American Chemical Society, 1983
- Enantioselective synthesis of the carbocyclic nucleosides (-)-aristeromycin and (-)-neplanocin A by a chemicoenzymatic approachJournal of the American Chemical Society, 1983
- Stereocontrolled synthesis of a cis-carbapenem antibiotic (-)-carpetimycin AJournal of the American Chemical Society, 1983
- Asymmetric hydrolysis of prochiral dimethyl 3-benzyloxycarbonylaminoglutarate with microorganisms. Preparation of (S)-3-amino-4-methoxycarbonylbutyric acid for the synthesis of carbapenem and negamycin antibiotics.Agricultural and Biological Chemistry, 1983
- Stereocontrolled synthesis of (+)-negamycin from an acyclic homoallylamine by 1,3-asymmetric inductionJournal of the American Chemical Society, 1982
- Chirally selective synthesis of sugar moiety of nucleosides by chemicoenzymatic approach: L- and D-riboses, showdomycin, and cordycepinJournal of the American Chemical Society, 1981
- Synthesis of (S)- and (R)-4[(methoxycarbonyl)methyl]-2-azetidinone by chemicoenzymic approachJournal of the American Chemical Society, 1981
- Ph3P-(PyS)2-CH3CN as an excellent condensing system for .beta.-lactam formation from .beta.-amino acidsJournal of the American Chemical Society, 1981