Enzymatic ammoniolysis of amino acid derivatives

M.C. de Zoete; A.A. Ouwehand; F. van Rantwijk; R.A. Sheldon

doi:10.1002/recl.19951140408

Enzymatic ammoniolysis of amino acid derivatives

M.C. de Zoete, A.A. Ouwehand, F. van Rantwijk, R.A. Sheldon

Research output: Contribution to journal › Article › Academic

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Abstract

The ammoniolysis of amino acid esters and their derivatives was performed with lipases and proteases yielding the corresponding amino acid amides with moderate to high enantioselectivity. Phenylglycine methyl ester racemized slowly under the reaction conditions.

Original language	English
Pages (from-to)	171-174
Journal	Recueil des travaux chimiques des Pays-Bas = Journal of the Royal Netherlands Chemical Society
Volume	114
Issue number	4-5
DOIs	https://doi.org/10.1002/recl.19951140408
Publication status	Published - 1995

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@article{34015e4114354feab5238c38cf6bea0f,

title = "Enzymatic ammoniolysis of amino acid derivatives",

abstract = "The ammoniolysis of amino acid esters and their derivatives was performed with lipases and proteases yielding the corresponding amino acid amides with moderate to high enantioselectivity. Phenylglycine methyl ester racemized slowly under the reaction conditions.",

author = "{de Zoete}, M.C. and A.A. Ouwehand and {van Rantwijk}, F. and R.A. Sheldon",

year = "1995",

doi = "10.1002/recl.19951140408",

language = "English",

volume = "114",

pages = "171--174",

journal = "Recueil des travaux chimiques des Pays-Bas = Journal of the Royal Netherlands Chemical Society",

issn = "0165-0513",

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T1 - Enzymatic ammoniolysis of amino acid derivatives

AU - de Zoete, M.C.

AU - Ouwehand, A.A.

AU - van Rantwijk, F.

AU - Sheldon, R.A.

PY - 1995

Y1 - 1995

N2 - The ammoniolysis of amino acid esters and their derivatives was performed with lipases and proteases yielding the corresponding amino acid amides with moderate to high enantioselectivity. Phenylglycine methyl ester racemized slowly under the reaction conditions.

AB - The ammoniolysis of amino acid esters and their derivatives was performed with lipases and proteases yielding the corresponding amino acid amides with moderate to high enantioselectivity. Phenylglycine methyl ester racemized slowly under the reaction conditions.

U2 - 10.1002/recl.19951140408

DO - 10.1002/recl.19951140408

M3 - Article

SN - 0165-0513

VL - 114

SP - 171

EP - 174

JO - Recueil des travaux chimiques des Pays-Bas = Journal of the Royal Netherlands Chemical Society

JF - Recueil des travaux chimiques des Pays-Bas = Journal of the Royal Netherlands Chemical Society

IS - 4-5

ER -

Enzymatic ammoniolysis of amino acid derivatives

Abstract

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