“Carba” peptide bond surrogates: synthesis of Boc-L-Leu-…(CH2-CH2)-L-Phe-OH and Boc-LLeu-ψ-(CH2-CH2)-D-Phe-OH through a horner-emmons reaction.

This publication has 6 references indexed in Scilit:

• A general route to “carba” peptide bond replacements: Unequivocal synthesis of Boc-L-Phe-ψ(CH2-CH2)-L-Ala-OH and Boc-L-Phe-ψ(CH2-CH2)-D-Ala-OH.
  Tetrahedron Letters, 1990
• Peptide and pseudopeptide analogues of cholecystokinin, chemical modifications of the met28-gly29 region
  Tetrahedron, 1988
• An Efficient Synthesis of Optically Active α-(t-Butoxycarbonylamino)-aldehydes from α-Amino Acids
  Synthesis, 1983
• Wittig-Horner Reactions in Heterogeneous Media; 2¹. A Convenient Synthesis of α,β-Unsaturated Esters and Ketones using Weak Bases in Water
  Synthesis, 1983
• Alkylation of Diethyl 2-Oxoalkanephosphonates
  Synthesis, 1975
• The Utility of Phosphonate Carbanions in Olefin Synthesis
  Journal of the American Chemical Society, 1961