Synthesis of optically active alkynyl alcohols and α-hydroxy esters by microbial asymmetric hydrolysis of the corresponding acetates
- 1 January 1980
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 36 (1) , 91-96
- https://doi.org/10.1016/0040-4020(80)85030-7
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Synthesis and absolute configuration of (-)-methyl (E)-2,4,5-tetradecatrienoate, the sex attractant of the male dried bean weevilThe Journal of Organic Chemistry, 1978
- Synthesis of optically active alkynyl alcohols by microbial asymmetric hydrolysis of the corresponding acetatesTetrahedron Letters, 1978
- Asymmetric reduction. Reduction of acetylenic ketones with chiral hydride agentJournal of the American Chemical Society, 1977
- Synthetic studies on (2R,4'R,8'R)-.alpha.-tocopherol. Facile syntheses of optically active, saturated, acyclic isoprenoids via stereospecific [3,3] sigmatropic rearrangementsThe Journal of Organic Chemistry, 1976
- Biochemical resolution of racemic terpenes. VII. Microbial resolution of some racemic monocyclic alcohols.Agricultural and Biological Chemistry, 1975
- Biochemical resolution of racemic terpenes. VI. Microbial resolution of (.+-.)-1 and 2-decalols.Agricultural and Biological Chemistry, 1974
- Biochemical resolution of racemic terpenes. V. Microbial resolution of (.+-.)-borneols.Agricultural and Biological Chemistry, 1974
- Microbial Resolution of Racemic 2- and 3-AlkylcyclohexanolsAgricultural and Biological Chemistry, 1973
- Microbial Resolution of Racemic CarvomentholsAgricultural and Biological Chemistry, 1973
- Microbial Resolution of dl-IsopulegolAgricultural and Biological Chemistry, 1973