Development of an <i>o</i>-aminoanilide-mediated native chemical ligation-assisted DADA strategy for the synthesis of disulfide surrogate peptides.

Cui, Tingting; Li, Wen-Jie; Chen, Junyou; Zhao, Rui; Li, Yi-Ming

Development of an o-aminoanilide-mediated native chemical ligation-assisted DADA strategy for the synthesis of disulfide surrogate peptides.

Cui, Tingting; Li, Wen-Jie; Chen, Junyou; Zhao, Rui; Li, Yi-Ming.

Afiliação

Cui T; School of Food and Biological Engineering, Engineering Research Center of Bio-process, Ministry of Education, Hefei University of Technology, Hefei 230009, China. ymli@hfut.edu.cn.
Li WJ; School of Food and Biological Engineering, Engineering Research Center of Bio-process, Ministry of Education, Hefei University of Technology, Hefei 230009, China. ymli@hfut.edu.cn.
Chen J; School of Food and Biological Engineering, Engineering Research Center of Bio-process, Ministry of Education, Hefei University of Technology, Hefei 230009, China. ymli@hfut.edu.cn.
Zhao R; Department of Chemistry, University of Science and Technology of China, Hefei 230026, China.
Li YM; School of Food and Biological Engineering, Engineering Research Center of Bio-process, Ministry of Education, Hefei University of Technology, Hefei 230009, China. ymli@hfut.edu.cn.

Org Biomol Chem ; 21(3): 533-537, 2023 01 18.

Article em En | MEDLINE | ID: mdl-36533871

Assuntos

Dissulfetos; Peptídeos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Dissulfetos Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

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