Preparation of Arylmercapturic Acids by S-Arylation of N,N?-Diacetylcystine

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F09%3A00021449" target="_blank" >RIV/60461373:22310/09:00021449 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Preparation of Arylmercapturic Acids by S-Arylation of N,N?-Diacetylcystine

Original language description

A simple convenient method for the preparation of N-acetyl-S-arylcysteines based on Chan-Lam-Evans arylation of N,N?-diacetylcystine dimethyl ester with arylboronic acids is described and used to synthesize a series of arylmercapturic acids. Unlike copper mediated N-arylation, S-arylation of both cysteine and cystine derivatives did not proceed satisfactorily in the presence of air.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

Result was created during the realization of more than one project. More information in the Projects tab.

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2009

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

European Journal of Organic Chemistry

ISSN

1434-193X

e-ISSN

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Volume of the periodical

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Issue of the periodical within the volume

36

Country of publishing house

DE - GERMANY

Number of pages

5

Pages from-to

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UT code for WoS article

000273187700009

EID of the result in the Scopus database

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