Origins of π-face selectivity in the aldol reactions of chiral E-enol borinates: a computational study using transition state modelling.
- 1 January 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (3) , 685-696
- https://doi.org/10.1016/s0040-4020(01)86270-0
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- The rational design of highly stereoselective boron enolates using transition-state computer modeling: a novel, asymmetric anti aldol reaction for ketonesThe Journal of Organic Chemistry, 1992
- Enolboration. 2. Dicyclohexylchloroborane/triethylamine as a convenient reagent for regio- and stereoselective enolboration of representative classes of ketonesThe Journal of Organic Chemistry, 1992
- Conformational analysis of chiral alkenes and oxonium ions: ab initio molecular orbital calculations and an improved MM2 force fieldJournal of the American Chemical Society, 1991
- Transition-state modeling of the aldol reaction of boron enolates: a force field approachThe Journal of Organic Chemistry, 1990
- Macromodel—an integrated software system for modeling organic and bioorganic molecules using molecular mechanicsJournal of Computational Chemistry, 1990
- Conformations of cycloheptadecane. A comparison of methods for conformational searchingJournal of the American Chemical Society, 1990
- Allylic 1,3-strain as a controlling factor in stereoselective transformationsChemical Reviews, 1989
- An internal-coordinate Monte Carlo method for searching conformational spaceJournal of the American Chemical Society, 1989
- The multiple minimum problem in molecular modeling. Tree searching internal coordinate conformational spaceJournal of Computational Chemistry, 1988
- N,N'-dibenzyl-N,N'-ethylenetartramide: a rationally designed chiral auxiliary for the allylboration reactionJournal of the American Chemical Society, 1988