Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/97425
Title: N-to-C sequential ligation using peptidyl N,N-Bis(2-mercaptoethyl)amide building blocks
Authors: Liu, Chuan-Fa
Yang, Renliang.
Hou, Wen.
Zhang, Xiaohong.
Keywords: DRNTU::Science::Biological sciences
Issue Date: 2011
Source: Yang, R., Hou, W., Zhang, X., & Liu, C. F. (2012). N-to-C sequential ligation using peptidyl N,N-Bis(2-mercaptoethyl)amide building blocks. Organic letters, 14(1), 374-377.
Series/Report no.: Organic letters
Abstract: A novel N- to C-terminus sequential chemical ligation approach has been developed for protein synthesis. Key to this strategy is the relative stability of the N,N-bis(2-mercaptoethyl)amide (BMEA) to the conventional conditions of native chemical ligation. We have also found a new thiol additive for the BMEA-mediated ligation reaction. The usefulness of this approach was demonstrated in the syntheses of a medium-sized peptide and ubiquitin.
URI: https://hdl.handle.net/10356/97425
http://hdl.handle.net/10220/10577
ISSN: 1523-7060
DOI: 10.1021/ol2031284
Schools: School of Biological Sciences 
Rights: © 2011 American Chemical Society.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SBS Journal Articles

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