Peptide synthesis by a combination of solid-phase and solution methods III resin derivatives allowing minimum-racemization coupling of nα-protected amino acids
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (48) , 6741-6744
- https://doi.org/10.1016/s0040-4039(00)70665-4
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Use of esters of 2,5-diphenyl-2,3-dihydro-3-oxo-4-hydroxythiophene dioxide in solid phase peptide synthesis. A new procedure for attachment of the first amino acidJournal of the Chemical Society, Chemical Communications, 1987
- Suppression of side‐reactions during the attachment of FMOC‐amino acids to hydroxymethyl polymersRecueil des Travaux Chimiques des Pays-Bas, 1985
- Racemisation of activated, urethane-protected amino-acids by p-dimethyl-aminopyridine. Significance in solid-phase peptide synthesisJournal of the Chemical Society, Chemical Communications, 1981
- Tertiäres Phosphan/Tetrachlormethan, ein vielseitiges Reagens zur Chlorierung, Dehydratisierung und PN-VerknüpfungAngewandte Chemie, 1975
- Ether cleavage by triphenyldibromophosphoraneThe Journal of Organic Chemistry, 1972
- A convenient preparative method for esters of amino acidsAustralian Journal of Chemistry, 1972
- Solid-Phase Peptide Synthesis. III. An Improved Synthesis of Bradykinin*Biochemistry, 1964
- Studies in Organophosphorus Chemistry. I. Conversion of Alcohols and Phenols to Halides by Tertiary Phosphine DihalidesJournal of the American Chemical Society, 1964
- Solid Phase Peptide Synthesis. I. The Synthesis of a TetrapeptideJournal of the American Chemical Society, 1963