Mitsunobu-type alkylation of p-toluenesulfonamide. A convenient new route to primary and secondary amines

This publication has 11 references indexed in Scilit:

• N-Benzyltriflamide: A generally useful mitsunobu reagent for amine synthesis
  Tetrahedron Letters, 1995
• 2- and 4-Nitrobenzenesulfonamides: Exceptionally versatile means for preparation of secondary amines and protection of amines
  Tetrahedron Letters, 1995
• Carbon-carbon bond formation with new Mitsunobu reagents
  Tetrahedron Letters, 1995
• Novel reactivity of stabilized methylenetributylphosphorane: A new mitsunobu reagent
  Tetrahedron Letters, 1994
• N,N,N′,N′-Tetramethylazodicarboxamide (TMAD), A New Versatile Reagent for Mitsunobu Reaction. Its Application to Synthesis of Secondary Amines
  Chemistry Letters, 1994
• Application of the aza-Claisen rearrangement to the total synthesis of natural products: (-)-Isoiridomyrmecin
  Pure and Applied Chemistry, 1994
• 1,1′-(azodicarbonyl)dipiperidine-tributylphosphine, a new reagent system for mitsunobu reaction
  Tetrahedron Letters, 1993
• Synthesis of N-acyl-, N-sulfonyl-, and N-phosphinylphospha(PV)azenes by a redox-condensation reaction using amides, triphenylphosphine, and diethyl azodicarboxylate
  The Journal of Organic Chemistry, 1985
• Cleavage of sulfonamides with sodium naphthalene
  Journal of the American Chemical Society, 1967
• Investigation on the Sodium—Liquid Ammonia Cleavage of a Tosyl Protecting Group of Tosylamino Acids and Peptides¹
  The Journal of Organic Chemistry, 1966