Solid-phase synthesis of peptides using allylic anchoring groups 2. Palladium-catalysed cleavage of Fmoc-protected peptides

This publication has 12 references indexed in Scilit:

• Automated Allyl Cleavage for Continuous-Flow Synthesis of Cyclic and Branched Peptides
  Analytical Biochemistry, 1993
• Convergent solid-phase peptide synthesis
  Tetrahedron, 1993
• Convergent solid-phase peptide synthesis. XI. Synthesis and purification of protected peptide segments spanning the entire sequence of the uteroglobin monomer using the photolabile nbb-resin.
  Tetrahedron, 1993
• Use of BOP reagent for the suppression of diketopiperazine formation in boc/bzl solid-phase peptide synthesis
  Tetrahedron Letters, 1990
• Use of an allylic anchor group and of its palladium catalyzed hydrostannolytic cleavage in the solid phase synthesis of protected peptide fragments
  Tetrahedron Letters, 1989
• Simultaneous multiple synthesis of protected peptide fragments on ‘allyl’-functionalized cellulose disc supports
  Tetrahedron Letters, 1988
• Selective cleavage of the allyl and (allyloxy)carbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis
  The Journal of Organic Chemistry, 1987
• Tri-n-butyltin Hydride as Reagent in Organic Synthesis
  Synthesis, 1987
• Three-dimensional orthogonal protection scheme for solid-phase peptide synthesis under mild conditions
  Journal of the American Chemical Society, 1985
• A new amino protecting group removable by reduction. Chemistry of the dithiasuccinoyl (Dts) function
  Journal of the American Chemical Society, 1977