Diastereofacial selectivity in the aldol reactions of chiral α-methyl aldehydes: a computer modelling approach.

This publication has 52 references indexed in Scilit:

• Transition-state modeling of the aldol reaction of boron enolates: a force field approach
  The Journal of Organic Chemistry, 1990
• Theoretical evidence in support of the Anh–Eisenstein electronic model in controlling π-facial stereoselectivity in nucleophilic additions to carbonyl compounds
  Journal of the Chemical Society, Chemical Communications, 1990
• Stereochemistry of crotylboronate additions to .alpha.,.beta.-dialkoxy aldehydes
  The Journal of Organic Chemistry, 1985
• Highly Stereoselective Aldol Condensation Using an Enantioselective Chiral Enolate
  Angewandte Chemie International Edition in English, 1980
• Enhancement of 1,2‐Asymmetric Induction on C-C Linkage by Use of Chiral 2‐Butenylboronic Esters
  Angewandte Chemie International Edition in English, 1980
• Acyclic stereoselection. 2. Synthesis of 3-hydroxy-2-methyl- and 3-hydroxy-2,4-dimethylcarboxylic acids
  Journal of the American Chemical Society, 1977
• Semiempirical calculation of conformational structure of 2,4-disubstituted pentanes
  Collection of Czechoslovak Chemical Communications, 1968
• Conformational Analysis of Macromolecules. II. The Rotational Isomeric States of the Normal Hydrocarbons
  The Journal of Chemical Physics, 1966
• Conformational Energies of n-Alkanes and the Random Configuration of Higher Homologs Including Polymethylene
  Journal of the American Chemical Society, 1966
• Conformational Analysis. XVII.¹ The 1,3-Diaxial Methyl-Methyl Interaction²
  Journal of the American Chemical Society, 1961