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Angewandte Chemie - International Edition

Volumn 49, Issue 31, 2010, Pages 5318-5321

The mercaptomethyl group facilitates an efficient one-pot ligation at Xaa-Ser/Thr for (Glyco)peptide synthesis

(6) Hojo, Hironobu a Ozawa, Chinatsu a Katayama, Hidekazu a Ueki, Akiharu a Nakahara, Yuko a Nakahara, Yoshiaki a

a TOKAI UNIVERSITY (Japan)

Author keywords

Glycopeptides; Ligation; Peptide thioesters; Synthetic methods

Indexed keywords

CONTULAKIN-G; GLYCOPEPTIDES; HUMAN CALCITONIN; HYDROXY GROUPS; NATIVE CHEMICAL LIGATION; ONE POT; PEPTIDE SYNTHESIS; PEPTIDE THIOESTERS; SIDE-CHAIN; SYNTHETIC METHODS; THIOESTERS; THREONINE RESIDUES;

AMINO ACIDS; PHOSPHATASES; SYNTHESIS (CHEMICAL);

PEPTIDES;

CALCITONIN; GLYCOPEPTIDE; LIGAND; THIOL DERIVATIVE;

AMINO ACID SEQUENCE; ARTICLE; CHEMISTRY; HUMAN; MOLECULAR GENETICS; SYNTHESIS;

AMINO ACID SEQUENCE; CALCITONIN; GLYCOPEPTIDES; HUMANS; LIGANDS; MOLECULAR SEQUENCE DATA; SULFHYDRYL COMPOUNDS;

EID: 77954858506 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201000384 Document Type: Article

Times cited : (37)

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- The ligation at Val-Thr, Leu-Thr, and Tyr-Thr sites was also tested. The first one was unproductive, but the latter two were useful for ligation (see the Supporting Information).

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