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Pyroacm Resin: An Acetamidomethyl Derived Resin for Solid Phase Synthesis of Peptides through Side Chain Anchoring of C-Terminal Cysteine Residues

Authors
Juvekar, VinayakGong, Young Dae
Issue Date
19-Feb-2016
Publisher
AMER CHEMICAL SOC
Citation
ORGANIC LETTERS, v.18, no.4, pp 836 - 839
Pages
4
Indexed
SCI
SCIE
SCOPUS
Journal Title
ORGANIC LETTERS
Volume
18
Number
4
Start Page
836
End Page
839
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/14931
DOI
10.1021/acs.orglett.6b00115
ISSN
1523-7060
1523-7052
Abstract
The design, synthesis and utilization of an efficient acetamidomethyl derived resin for the peptide synthesis is presented using established Fmoc and Boc protocols via side chain anchoring. Cleavage of the target peptide from the resin is performed using carboxymethylsulfenyl chloride under mild conditions which gave in situ thiol-sulfenyl protection of the cysteine residues. The utility of the resin is successfully demonstrated through applications to the syntheses of model peptides and natural products Riparin 1.1 and Riparin 1.2.
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