Mild and rapid azide- mediated, palladium catalyzed cleavage of allylester based protecting groups

This publication has 20 references indexed in Scilit:

• On the use of silylated nucleophiles in the palladium catalysed deprotection of allylic carboxylates and carbamates.
  Tetrahedron Letters, 1992
• Improved protective groups for phosphate of o-phosphoserine useful for the solid-phase peptide synthesis
  Tetrahedron Letters, 1991
• Solid‐phase synthesis of peptides containing phosphoserine using phosphate tert.‐butyl protecting group*
  International Journal of Peptide and Protein Research, 1990
• 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
• Palladium-catalyzed reaction of tributyltin hydride. Selective and very mild deprotection of allyl and allyloxycarbonyl derivatives of amino-acids.
  Tetrahedron Letters, 1986
• THE CINNAMYLOXYCARBONYL GROUP AS A NEW AMINO-PROTECTING GROUP
  Chemistry Letters, 1985
• Palladium-catalyzed reaction of allyl carbamates; allylation of carbonucleophiles, and protection-deprotection of amines
  Tetrahedron Letters, 1985
• Redox-switched crown ethers monocrown-biscrown interconversion coupled with redox of a thiol-disulfide couple
  Tetrahedron Letters, 1982
• The allyloxycarbonyl group for alcohol protection: quantitative removal or transformation into allyl protecting group via π-allyl complexes of palladium
  Tetrahedron Letters, 1981
• New rules of selectivity: allylic alkylations catalyzed by palladium
  Accounts of Chemical Research, 1980