Asymmetric [2,3]wittig rearrangement of 2′-alkenyloxyacetamide bearing -2,5-bis(methoxymethoxymethyl)pyrrolidine moiety as a chiral auxiliary

This publication has 12 references indexed in Scilit:

• Asymmetric aldol reaction of amide enolates bearing trans-2,5-disubstituted pyrrolidines as chiral auxiliaries
  Tetrahedron Letters, 1985
• A highly effective asymmetric synthesis of α-hydroxy acids by alkylation of chiral n-(benzyloxyacetyl)-trans-2,5-bis(methoxymethoxymethyl)pyrrolidine
  Tetrahedron Letters, 1985
• ASYMMETRIC [2,3]WITTIG SIGMATROPIC REARRANGEMENTS INVOLVING CHIRAL AMIDE ENOLATES AS THE MIGRATING TERMINI
  Chemistry Letters, 1985
• Highly -diastereoselective reduction of 2-alkyl-3-oxo amides by potassium triethylborohydride
  Tetrahedron Letters, 1985
• Asymmetric alkylation of carboxyamides by using trans-2,5-disubstituted pyrrolidines as chiral auxiliaries
  Tetrahedron Letters, 1984
• Asymmetric acylation of carboxamides having -2,5-bis(methoxymethoxymethyl)pyrrolidine moiety as a chiral auxiliary and stereoselective reduction of the resulting 2-alkyl-3-oxoamides
  Tetrahedron Letters, 1984
• Intramolecular acylation of vinylic silanes. A novel, general approach for the synthesis of four- to six-membered carbocyclic systems and its regiochemical features
  Tetrahedron Letters, 1983
• The [2,3]Wittig rearrangement of 2-alkenyloxyacetic acids and its applications to the stereocontrolled synthesis of β, γ-unsaturated aldehydes and conjugated dienoic acids
  Tetrahedron Letters, 1981
• A simple approach to 1-azaspiro[4,5]decanes
  The Journal of Organic Chemistry, 1979
• Studies on Diastereoisomeric α-Amino Acids and Corresponding α-Hydroxy Acids. VII. Influence of β-Configuration on Enzymic Susceptibility
  Journal of the American Chemical Society, 1956