DIPHENYL PHOSPHONATE ESTER CLEAVAGE CATALYZED BY HYDROPHOBIC AMMONIUM IONS

DOI: 10.1016/S0040-4020(01)90015-8

Source and publish data:

Tetrahedron p. 799 - 804 (1987)

Update date:2022-08-04

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Authors:

Kafarski, Pawel

Lejczak, Barbara

Plucinski, Pawel

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Article abstract of DOI:10.1016/S0040-4020(01)90015-8

The basic hydrolysis of diphenyl <1-(N-benzyloxy-carbonylalanyl)-3-methyl>butylphosphonate have been studied in various cationic micelles.The kinetics of the reactions in buffered solutions and dilute sodium hydroxide solutions are compared.

Full text of DOI:10.1016/S0040-4020(01)90015-8

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Product name:Carbamic acid, [2-[[1-(hydroxyphenoxyphosphinyl)-3-methylbutyl]amino]-1-methyl-2-oxo ethyl]-, phenylmethyl ester

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