Synfacts 2024; 20(11): 1230
DOI: 10.1055/s-0043-1775112
Peptide Chemistry

FCDMT-Mediated Peptide Synthesis

Rezensent(en):
Hisashi Yamamoto
,
Isai Ramakrishna
Markowicz MW, Dembinski R. * Oakland University, Rochester, USA
Fluorous Coupling Reagents: Application of 2-Chloro-4,6-bis[(heptadecafluorononyl)oxy]-1,3,5-triazine in Peptide Synthesis.

Synthesis 2004; 80-86
DOI: 10.1055/s-2003-42492
 

Significance

Development of eco-friendly, cost-effective, and practically easy coupling reagents for peptide synthesis is a highly demanding area of peptide drugs discovery. In this study, the authors invented 2-chloro-4,6-bis[(heptadecafluoro-nonyl)oxy]-1,3,5-triazine as an efficient coupling reagent for the synthesis of various peptides.


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Comment

Various peptides were synthesized by the coupling between N-benzyloxycarbonyl amino acids and amino acid methyl esters with the help of 2-chloro-4,6-bis[(heptadecafluorononyl)oxy]-1,3,5-triazine. The protocol is practically simple and suitable for the synthesis of peptides having ­sterically hindered α,α-disubstituted amino acids.


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Publikationsverlauf

Artikel online veröffentlicht:
16. Oktober 2024

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