Your browser doesn't support javascript.
loading
Robust synthesis of C-terminal cysteine-containing peptide acids through a peptide hydrazide-based strategy.
Zuo, Chao; Yan, Bing-Jia; Zhu, Han-Ying; Shi, Wei-Wei; Xi, Tong-Kuai; Shi, Jing; Fang, Ge-Min.
Affiliation
  • Zuo C; School of Life Science, Institute of Health Science and Technology, Institutes of Physical Science and Information Technology, Anhui University, Hefei 230601, PR China. fanggm@ahu.edu.cn.
Org Biomol Chem ; 17(23): 5698-5702, 2019 06 12.
Article de En | MEDLINE | ID: mdl-31135013
ABSTRACT
A new robust strategy was reported for the epimerization-free synthesis of C-terminal Cys-containing peptide acids through mercaptoethanol-mediated hydrolysis of peptide thioesters prepared in situ from peptide hydrazides. This simple-to-operate and highly efficient method avoids the use of derivatization reagents for resin modification, thus providing a practical avenue for the preparation of C-terminal Cys-containing peptide acids.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Peptides / Acides / Cystéine Langue: En Journal: Org Biomol Chem Sujet du journal: BIOQUIMICA / QUIMICA Année: 2019 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Peptides / Acides / Cystéine Langue: En Journal: Org Biomol Chem Sujet du journal: BIOQUIMICA / QUIMICA Année: 2019 Type de document: Article