A convenient method for enzymatic benzyl-alkyl transesterification under mild neutral conditions

Arie L. Gutman; Eleonora Shkolnik; Michal Shapira

doi:10.1016/S0040-4020(01)89450-3

A convenient method for enzymatic benzyl-alkyl transesterification under mild neutral conditions

Arie L. Gutman, Eleonora Shkolnik, Michal Shapira

Research output: Contribution to journal › Article › peer-review

17 Scopus citations

Abstract

Lipases from Candida cylindracea and from Pseudomonas fluorescens efficiently catalyse the benzyl to alkyl transesterification in organic solvents under mild conditions in nearly quantitative yields.

Original language	English
Pages (from-to)	8775-8780
Number of pages	6
Journal	Tetrahedron
Volume	48
Issue number	40
DOIs	https://doi.org/10.1016/S0040-4020(01)89450-3
State	Published - 1992
Externally published	Yes

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10.1016/S0040-4020(01)89450-3

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title = "A convenient method for enzymatic benzyl-alkyl transesterification under mild neutral conditions",

abstract = "Lipases from Candida cylindracea and from Pseudomonas fluorescens efficiently catalyse the benzyl to alkyl transesterification in organic solvents under mild conditions in nearly quantitative yields.",

author = "Gutman, {Arie L.} and Eleonora Shkolnik and Michal Shapira",

year = "1992",

doi = "10.1016/S0040-4020(01)89450-3",

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AU - Gutman, Arie L.

AU - Shkolnik, Eleonora

AU - Shapira, Michal

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N2 - Lipases from Candida cylindracea and from Pseudomonas fluorescens efficiently catalyse the benzyl to alkyl transesterification in organic solvents under mild conditions in nearly quantitative yields.

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AN - SCOPUS:0026733769

SN - 0040-4020

VL - 48

SP - 8775

EP - 8780

JO - Tetrahedron

JF - Tetrahedron

IS - 40

ER -

A convenient method for enzymatic benzyl-alkyl transesterification under mild neutral conditions

Abstract

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