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- Ozone-mediated reaction of anilides and phenyl esters with nitrogen dioxide: enhanced ortho-reactivity and mechanistic implications. Hitomi Suzuki, Atsuo Tatsumi, Taro Ishibashi, Tadashi Mori
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 339
- Nucleophilic versus general base catalysis in phosphyl (PV) group transfer: application to α-chymotrypsin action. Kenneth T. Douglas, Andrew Williams
, J. Chem. Soc., Perkin Trans. 2
, 1976
, 515
- K2CO3-promoted formation of aryl esters from primary aryl amides by the acyl–acyl exchange process. Yongjun Bian, Xingyu Qu
, Org. Biomol. Chem.
, 2016
, 14
, 3869
- Proteolytic enzymes: lipophilic binding sites for specific and non-specific substrates of α-chymotrypsin. Janos Udris, Andrew Williams
, J. Chem. Soc., Perkin Trans. 2
, 1976
, 686
- Effects of substituents on the hydrolysis of 4-nitrophenyl acetate catalysed by 2-substituted imidazoles. Masayasu Akiyama, Yukihiro Hara, Minoru Tanabe
, J. Chem. Soc., Perkin Trans. 2
, 1978
, 288
- Investigation of the applicability of cis-urocanic acid as a model for the catalytic Asp–His dyad in the active site of serine proteases based on 1H NMR hydrogen bonding studies and spectroscopic pK
a measurements. Helmi Neuvonen, Kari Neuvonen
, J. Chem. Soc., Perkin Trans. 2
, 1998
, 1665
- The carboxypeptidase Y-catalysed hydrolysis of aryl trimethylacetates: the nature of the deacylation reaction of trimethylacetylcarboxypeptidase Y. Kenneth T. Douglas, Yasushi Nakagawa, E. Thomas Kaiser
, J. Chem. Soc., Chem. Commun.
, 1975
, 429