Tandem deprotection-coupling of Nα-Alloc-amino acids by use of ternary systems Pd cat./PhSiH3/carboxy-activated amino acid
- 26 March 1999
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 40 (13) , 2505-2508
- https://doi.org/10.1016/s0040-4039(99)00240-3
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Use of Alloc-amino acids in solid-phase peptide synthesis. Tandem deprotection-coupling reactions using neutral conditionsPublished by Elsevier ,1998
- Allylic protecting groups and their use in a complex environment part II: Allylic protecting groups and their removal through catalytic palladium π-allyl methodologyTetrahedron, 1998
- Protected amino acid chlorides vs protected amino acid fluorides: Reactivity comparisonsTetrahedron Letters, 1998
- Peptide Synthesis via Amino Acid HalidesAccounts of Chemical Research, 1996
- Palladium catalyzed reductive deprotection of Alloc: Transprotection and peptide bond formationTetrahedron Letters, 1995
- Palladium-Catalyzed Transprotection of Allyloxycarbonyl-Protected Amines: Efficient One-Pot Formation of Amides and DipeptidesThe Journal of Organic Chemistry, 1995
- Urethane protected amino acid N-carboxyanhydrides and their use in peptide synthesisJournal of the American Chemical Society, 1990