Synthesis of peptide thioesters via an N-S acyl shift reaction under mild acidic conditions on an N-4,5-dimethoxy-2-mercaptobenzyl auxiliary group

Journal of Peptide Science

Volumn 15, Issue 11, 2009, Pages 731-737

  Nakamura, Ken'ichiroh ^a   Kanao, Tomoki ^a   Uesugi, Tomoya ^a   Hara, Toshiaki ^a   Sato, Takeshi ^a   Kawakami, Toru ^a   Aimoto, Saburo ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

4,5 dimethoxy 2 mercaptobenzyl (Dmmb) group; Fmoc SPPS; N S acyl shift; On resin preparation; Peptide thioester; Thioester producing resin

Indexed keywords

AMINO ACID; BENZYL DERIVATIVE; LEUCINE; LYSINE; MESNA; N 4,5 DIMETHOXY 2 MERCAPTOBENZYL DERIVATIVE; PEPTIDE DERIVATIVE; RESIN; THIOESTER; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; EPIMERIZATION; PEPTIDE SYNTHESIS; PHOSPHORYLATION; PRIORITY JOURNAL; RACEMIZATION;

ESTERS; PEPTIDES; SULFHYDRYL COMPOUNDS; TRIFLUOROACETIC ACID;

EID: 70449636047     PISSN: 10752617     EISSN: 10991387     Source Type: Journal    
DOI: 10.1002/psc.1164     Document Type: Article

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