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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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