Amide Hydrolysis
Amide Hydrolysis is a chemical reaction, classified as a nucleophilic acyl substitution, in which an amide undergoes cleavage in the presence of water under acidic or basic conditions to yield a carboxylic acid and an amine or ammonia.
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2017–2026
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Mechanism of C-terminal amide formation by pituitary enzymes
A.F. Bradbury, M. D. A. FINNIE, D.G. Smyth · Nature · 1982 · 661 citations
Darren Fegley, Silvana Gaetani, Andrea Duranti et al. · Journal of Pharmacology and Experimental Therapeutics · 2005 · 430 citations · Full text
Medicine, Neuroscience, Pharmacology +11
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Massachusetts Institute of Technology, United States
36 publications · 2.4K citations
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Massachusetts Institute of Technology
Cambridge, United States
31 h-index
91 publications
6.4K citations
Scripps Research Institute
San Diego, United States
22 h-index
86 publications
10.9K citations

Kyoto University
Kyoto, Japan
13 h-index
52 publications
1.6K citations
Harvard University
Cambridge, United States
12 h-index
33 publications
3.4K citations
Pfizer (United States)
New York, United States
11 h-index
70 publications
6.2K citations
KU Leuven
Leuven, Belgium
11 h-index
41 publications
1.7K citations
University of Stuttgart
Stuttgart, Germany
10 h-index
28 publications
1.3K citations
University of Pennsylvania
Philadelphia, United States
10 h-index
26 publications
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JBC · 85 publications · 6.2K citations
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JACS · 96 publications · 5.2K citations
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JOC · 35 publications · 1.3K citations
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