Baker's yeast reduction of β-keto esters in petrol
- 4 March 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (10) , 1699-1702
- https://doi.org/10.1016/0040-4039(96)00111-6
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- The Use of Organic Solvent Systems in the Yeast Mediated Reduction of Ethyl AcetoacetateBulletin of the Chemical Society of Japan, 1994
- Total Synthesis of Grahamimycin A1Bulletin of the Chemical Society of Japan, 1993
- An improved procedure for the synthesis and use of [RuCl2(BINAP)]2.cntdot.NEt3. Dependence of the ruthenium(II)-BINAP catalyzed asymmetric hydrogenation of .beta.-keto esters on trace amounts of acidThe Journal of Organic Chemistry, 1992
- Asymmetric reductions of prochiral ketones with B-3-pinanyl-9-borabicyclo[3.3.1]nonane (Alpine-Borane) at elevated pressuresThe Journal of Organic Chemistry, 1989
- Asymmetric synthesis of (1'R,3R,4R)-4-acetoxy-3-[1'-((tert-butyldimethylsilyl)oxy)ethyl]-2-azetidinone and other 3-(1'-hydroxyethyl)-2-azetidinones from (S)-(+)-ethyl 3-hydroxybutanoate: formal total synthesis of (+)-thienamycinJournal of the American Chemical Society, 1987
- Stereo- and enantio-controlled synthesis of chiral intermediates for the total synthesis of thienamycin and related β-lactam antibiotics from 3-hydroxybutyratesJournal of the Chemical Society, Chemical Communications, 1985
- C45‐ and C50‐Carotinoide. 1. Mitteilung. Synthese von (R)‐ and (S)‐LavandulolHelvetica Chimica Acta, 1982
- Synthesis of Three Stereoisomeric Forms of 2,8-Dimethyl-1,7-dioxaspiro[5.5]undecane, the Main Component of the Cephalic Secretion of Andrena wilkellaHETEROCYCLES, 1981
- Über die Stereoselektivität der α‐Alkylierung von (1R, 2S) (+)‐cis‐2‐hydroxy‐cyclohexancarbonsäureäthylesterHelvetica Chimica Acta, 1980
- Über die Stereospezifität der α‐Alkylierung von β‐Hydroxycarbonsäureestern. Vorläufige MitteilungHelvetica Chimica Acta, 1979