Asymmetric synthesis of pre-protected α,α-disubstituted amino acids from tert-butanesulfinyl ketimines

This publication has 8 references indexed in Scilit:

• Synthesis of Enantiomerically Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-Butanesulfinamide with Aldehydes and Ketones
  The Journal of Organic Chemistry, 1999
• Synthesis of (S)- and (R)-1-(2-Furyl)alkylamines and (S)- and (R)-α-Amino Acids Through the Addition of Organometallic Reagents to Imines Derived from (S)-Valinol
  Synthesis, 1998
• Asymmetric Synthesis of α,α-Dibranched Amines by the Trimethylaluminum-Mediated 1,2-Addition of Organolithiums to tert-Butanesulfinyl Ketimines
  Journal of the American Chemical Society, 1998
• Stereoselective synthesis of quaternary α-amino acids. Part 1: Acyclic compounds
  Tetrahedron: Asymmetry, 1998
• tert-Butylsulfonyl (Bus), a New Protecting Group for Amines
  The Journal of Organic Chemistry, 1997
• Heteroarene-2-sulfonyl Chlorides (BtsCl; ThsCl): Reagents for Nitrogen Protection and >99% Racemization-Free Phenylglycine Activation with SOCl₂
  Journal of the American Chemical Society, 1996
• Non-standard amino acids in peptide design and protein engineering
  Current Opinion in Structural Biology, 1992
• The design of metabolically-stable peptide analogs
  Trends in Neurosciences, 1985