Synthesis of diacylamines and the preparation of α-amino-acylureas, a new type of α-amino acid derivatives

Imre Weisz; John Roboz; Imre Wolf; Jozsef Szabo; J. George Bekesi

doi:10.1016/S0960-894X(98)00593-9

Synthesis of diacylamines and the preparation of α-amino-acylureas, a new type of α-amino acid derivatives

Imre Weisz
, John Roboz
, Imre Wolf
, Jozsef Szabo
, J. George Bekesi

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

2 Scopus citations

Abstract

Sixteen new and one known unsymmetrical open-chain diacylamines were synthesized by sodium methoxide catalyzed acylation of amides with carboxylic esters and acylamino-carboxylic esters, or acylureas with acylamino- carboxylic esters and α-amino acid esters.

Original language	English
Pages (from-to)	3241-3244
Number of pages	4
Journal	Bioorganic and Medicinal Chemistry Letters
Volume	8
Issue number	22
DOIs	https://doi.org/10.1016/S0960-894X(98)00593-9
State	Published - 17 Nov 1998

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title = "Synthesis of diacylamines and the preparation of α-amino-acylureas, a new type of α-amino acid derivatives",

abstract = "Sixteen new and one known unsymmetrical open-chain diacylamines were synthesized by sodium methoxide catalyzed acylation of amides with carboxylic esters and acylamino-carboxylic esters, or acylureas with acylamino- carboxylic esters and α-amino acid esters.",

author = "Imre Weisz and John Roboz and Imre Wolf and Jozsef Szabo and Bekesi, \{J. George\}",

year = "1998",

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T1 - Synthesis of diacylamines and the preparation of α-amino-acylureas, a new type of α-amino acid derivatives

AU - Weisz, Imre

AU - Roboz, John

AU - Wolf, Imre

AU - Szabo, Jozsef

AU - Bekesi, J. George

PY - 1998/11/17

Y1 - 1998/11/17

N2 - Sixteen new and one known unsymmetrical open-chain diacylamines were synthesized by sodium methoxide catalyzed acylation of amides with carboxylic esters and acylamino-carboxylic esters, or acylureas with acylamino- carboxylic esters and α-amino acid esters.

AB - Sixteen new and one known unsymmetrical open-chain diacylamines were synthesized by sodium methoxide catalyzed acylation of amides with carboxylic esters and acylamino-carboxylic esters, or acylureas with acylamino- carboxylic esters and α-amino acid esters.

UR - https://www.scopus.com/pages/publications/0032541988

U2 - 10.1016/S0960-894X(98)00593-9

DO - 10.1016/S0960-894X(98)00593-9

M3 - Article

C2 - 9873710

AN - SCOPUS:0032541988

SN - 0960-894X

VL - 8

SP - 3241

EP - 3244

JO - Bioorganic and Medicinal Chemistry Letters

JF - Bioorganic and Medicinal Chemistry Letters

IS - 22

ER -

Synthesis of diacylamines and the preparation of α-amino-acylureas, a new type of α-amino acid derivatives

Abstract

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