Enantioselective routes toward 1β-methylcarbapenems from chiral aziridines
- 1 January 1992
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 48 (29) , 6079-6086
- https://doi.org/10.1016/s0040-4020(01)89856-2
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Reductive cleavage of tert-butyldimethylsilyl ethers by diisobutylaluminum hydrideThe Journal of Organic Chemistry, 1992
- Chiral synthesis of the key intermediate for 1β-methylcarbapenem antibiotics starting from (–)-carvoneJournal of the Chemical Society, Perkin Transactions 1, 1991
- A novel ring-closure strategy for the carbapenems: the total synthesis of (+)-thienamycinThe Journal of Organic Chemistry, 1990
- Stereocontrolled synthesis of an important intermediate for the preparation of 1.beta.-methylcarbapenem antibioticsThe Journal of Organic Chemistry, 1987
- Synthetic Carbapenem Antibiotics. I. 1-b-MethylcarbapenemHETEROCYCLES, 1984
- Syntheses of Optically Active Verrucarinic Acid. 40th Communication on Verrucarins and RoridinsHelvetica Chimica Acta, 1983
- Thienamycin total synthesis: stereocontrolled introduction of the hydroxyethyl side chainThe Journal of Organic Chemistry, 1981
- A stereocontrolled synthesis of (+)-thienamycinJournal of the American Chemical Society, 1980
- Structure and absolute configuration of thienamycinJournal of the American Chemical Society, 1978
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969