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- W2042987384 abstract "The aqueous solution chemistry of the C-3'-acetoxy moiety of cephalothin sodium (1b) was examined with the use of isotopically labeled H2(18)O and [2-13C]acetate anion. The 18O incorporation studies indicate that the hydrolysis (at pH 4.7 +/- 0.1) of 1b to the deacetyl derivative of cephalothin (2b) proceeds via two pathways: alkyl-oxygen bond cleavage (55-63%) and acyl-oxygen bond cleavage accounting for the remainder. The incorporation of [2-13C]acetate into 1b suggests that the alkyl-oxygen cleavage pathway is a reversible reaction." @default.
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- W2042987384 date "1985-11-01" @default.
- W2042987384 modified "2023-09-27" @default.
- W2042987384 title "Cephalothin: Hydrolysis of the C-3′-Acetoxy Moiety of a 7-Aminocephalosporanic Acid; Observation of both Acyl-oxygen Bond Cleavage and Reversible Alkyl-oxygen Bond Cleavage" @default.
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- W2042987384 doi "https://doi.org/10.1002/jps.2600741106" @default.
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