Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 130, Issue 47, Pages 15814-+Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja804993y
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Funding
- National Institutes of Health [CA28824]
- SKI [CA02848]
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A direct oxo-ester peptide ligation method has been developed. Through the use of an activated C-terminal para nitrophenyl ester (1), it is possible to achieve direct cysteine ligations (1 + 2 -> 4). Peptide substrates incorporating bulky C-terminal amino acids (1) can be accommodated with high reaction efficiency.
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