Stereodivergent synthesis of the enolates of a β-amino ester by using lithium N-benzyltrimethylsilylamide

This publication has 15 references indexed in Scilit:

• Aminolead compounds as a new reagent for regioselective ring opening of epoxides
  Tetrahedron Letters, 1989
• Stereoselective α-alkylation of α,β-unsaturated esters utilizing conjugate addition of nitrogen nucleophiles (R₂NLi)
  Journal of the Chemical Society, Chemical Communications, 1987
• High diastereoface selection in an ester enolate addition to .alpha.-alkoxy aldehydes: stereoselective synthesis of .alpha.-methylene-.beta.-hydroxy-.gamma.-alkoxy esters
  The Journal of Organic Chemistry, 1984
• Stereoselective synthesis of α-methylene-β-hydroxy-γ-alkoxy esters from α-alkoxy aldehydes
  Journal of the Chemical Society, Chemical Communications, 1983
• Staggered models for asymmetric induction: attack trajectories and conformations of allylic bonds from ab initio transition structures of addition reactions
  Journal of the American Chemical Society, 1982
• Ph3P-(PyS)2-CH3CN as an excellent condensing system for .beta.-lactam formation from .beta.-amino acids
  Journal of the American Chemical Society, 1981
• The 2-Phenylselenenylation of 2-Enoic Esters
  Synthetic Communications, 1980
• The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation
  Journal of the American Chemical Society, 1976
• Deconjugative alkylation of the enolate anion derived from ethyl crotonate
  Tetrahedron Letters, 1973
• Über die Konstellation der epimeren 1‐Amino‐1.2‐diphenyl‐propanole‐(3)
  European Journal of Inorganic Chemistry, 1965