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- Thomas, Gemma L. (author)
Peptide ligations accelerated by N-terminal aspartate and glutamate residues.
- Article/chapterEnglish2011
Publisher, publication year, extent ...
- 2011-08-10
- American Chemical Society (ACS),2011
- printrdacarrier
Numbers
- LIBRIS-ID:oai:DiVA.org:kth-211526
- https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-211526URI
- https://doi.org/10.1021/ol2017356DOI
Supplementary language notes
- Language:English
- Summary in:English
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- SwePubSwePub
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Notes
- QC 20170807
- A novel application of intramolecular base catalysis confers enhanced reaction rates for aminolysis ligations between peptide thioesters and peptides bearing N-terminal aspartate or glutamate residues. The broad scope of this process and its application in the total synthesis of the diabetes drug exenatide is demonstrated.
Subject headings and genre
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- Hsieh, Yves S. Y.University of Sydney, Australia(Swepub:kth)u1a596wi (author)
- Chun, Candy K. Y. (author)
- Cai, Zheng-Li (author)
- Reimers, Jeffrey R. (author)
- Payne, Richard J. (author)
- University of Sydney, Australia (creator_code:org_t)
Related titles
- In:Organic Letters: American Chemical Society (ACS)13:18, s. 4770-31523-70601523-7052
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- Royal Institute of Technology
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