Highly diastereoselective intramolecular nitrone cycloadditions to α,β-unsaturated esters.
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (23) , 2881-2884
- https://doi.org/10.1016/0040-4039(88)85237-7
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Highly stereocontrolled synthesis of the key intermediate of 1β-methylcarbapenem antibiotic via intramolecular nitrone 1,3-dipolar cycloadditionJournal of the Chemical Society, Chemical Communications, 1988
- A Chiral Synthesis of the Key Intermediate of 1b-Methylcarbapenem AntibioticHETEROCYCLES, 1988
- Nitrone Cycloaddition Route to the 1β-Methylcarbapenem Key IntermediateBulletin of the Chemical Society of Japan, 1987
- Enantioselective Syntheses of Carbapenem AntibioticsHETEROCYCLES, 1987
- Asymmetric Synthesis of 4-Acetoxy-3-hydroxyethylazetidin-2-one, a Key Intermediate for the Preparation of Penem and Carbapenem AntibioticsHETEROCYCLES, 1987
- Chiral synthesis of the key intermediate of (+)- and (-)-thienamycinThe Journal of Organic Chemistry, 1985
- The stereoselectivity of addition of N-benzyl-C-alkylnitrones to methyl crotonate. X-Ray crystal structure of (3RS,4SR,5RS)-2-benzyl-4-methoxy-carbonyl-5-methyl-3-[(4RS)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]isoxazolidineJournal of the Chemical Society, Perkin Transactions 1, 1985
- Further studies on the synthesis of thienamycin: a facile and stereoselective synthesis of a bicyclic .beta.-keto ester by 1,3-dipolar cycloadditionThe Journal of Organic Chemistry, 1982
- An efficient stereoselective method for the synthesis of thienamycin intermediatesJournal of the Chemical Society, Chemical Communications, 1982
- Thienamycin. A solution of the stereochemical problemTetrahedron Letters, 1979