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- W2014900089 abstract "Penicillin G acylase (PGA) accepts in toluene several analogues of phenylacetic acid as acyl donors. The 4-hydroxyphenylacetic group is preferentially accepted, and steric factors, such as the substitution at the aromatic ring or at the methylene group, cause a remarkable reduction in the initial rates. Results indicate that the selectivity follows a similar trend both in toluene and in aqueous media and that the synthetic potential of PGA can be fully exploited also in non-aqueous media with the consequent advantages, such as the absence of competitive hydrolytic reactions, higher solubility of phenylacetic derivatives and the possibility of working with equimolar amounts of reactants." @default.
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- W2014900089 date "2001-12-01" @default.
- W2014900089 modified "2023-09-27" @default.
- W2014900089 title "Selectivity of penicillin G acylase towards phenylacetic acid derivatives in amide bond synthesis in toluene" @default.
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- W2014900089 doi "https://doi.org/10.1016/s1381-1177(01)00047-9" @default.
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