Diastereoselectivity in theLewis acid mediated aldol reaction of chiral α, β-epoxyaldehydes with a ketene silyl acetal

This publication has 22 references indexed in Scilit:

• Diastereoface differentiation in addition of lithium enolates to chiral α,β-epoxyaldehydes
  Tetrahedron, 1993
• A rapid injection NMR study of the chelation controlled Mukaiyama aldol addition: TiCl4 versus LiClO4 as the Lewis acid
  Tetrahedron, 1992
• On the origin of π-facial diastereoselectivity in nucleophilic additions to chiral carbonyl compounds. 1. Rotational profiles of propionaldehyde 1, chloroacetaldehyde 2, and 2-chloropropionaldehyde 3.
  Tetrahedron, 1991
• Acyclic stereoselection. 32. Synthesis and characterization of the diastereomeric (4S)-pentane-1,2,3,4-tetraols
  The Journal of Organic Chemistry, 1985
• Chelation or Non‐Chelation Control in Addition Reactions of Chiral α‐ and β‐ Alkoxy Carbonyl Compounds [New Synthetic Methods (44)]
  Angewandte Chemie International Edition in English, 1984
• The Aldol Addition Reaction
  Published by Elsevier ,1984
• Total synthesis of carbohydrates. 2. Regiochemical control of nucleophilic ring opening of acylated 2,3-epoxy alcohols
  The Journal of Organic Chemistry, 1983
• Stereocontrolled total synthesis of (.+-.)-maytansinol
  Journal of the American Chemical Society, 1982
• Chelation-controlled nucleophilic additions. 1. A highly effective system for asymmetric induction in the reaction of organometallics with α-alkoxyketones.
  Tetrahedron Letters, 1980
• The Stereochemistry of the Ivanov and Reformatsky Reactions. I
  Journal of the American Chemical Society, 1957