Functionally Substituted Isothiazole- and Isoxazolecarboxamides


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Convenient synthetic approaches to functionally substituted 5-phenyl-1,2-oxazole-3-carboxamides and 4,5-dichloro-1,2-thiazole-3-carboxamides were developed on the basis of reactions of the corresponding carboxylic acid chlorides with primary aromatic and aliphatic amines. Optimal ratios acid chloride—amine (or amine hydrochloride)–triethylamine were found so that the reaction did not involve active chlorine atom in position 5 of the isothiazole ring.

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E. Dikusar

Institute of Physical Organic Chemistry

编辑信件的主要联系方式.
Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk

S. Petkevich

Institute of Physical Organic Chemistry

Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk

N. Zhukovskaya

Institute of Physical Organic Chemistry

Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk

T. Zvereva

Institute of Physical Organic Chemistry

Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk

P. Kurman

Institute of Bioorganic Chemistry

Email: dikusar@ifoch.bas-net.by
白俄罗斯, Minsk

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