Alkylation of 4-(phenylthio)-1H-pyrazol-5-ols with methyl bromoacetate


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详细

Alkylation of 4-(phenylthio)-1H-pyrazol-5-ols with methyl bromoacetate has afforded a series of phenyl pyrazolyl sulfides which have been oxidized into sulfones. The resulting esters have been hydrolyzed into the corresponding acids. The synthesized compounds potentially exhibit biological activity.

作者简介

R. Vydzhak

Institute of Bioorganic Chemistry and Petrochemistry

Email: brovarets@bpci.kiev.ua
乌克兰, ul. Murmanskaya 1, Kyiv, 02660

S. Panchishin

Institute of Bioorganic Chemistry and Petrochemistry

Email: brovarets@bpci.kiev.ua
乌克兰, ul. Murmanskaya 1, Kyiv, 02660

V. Brovarets

Institute of Bioorganic Chemistry and Petrochemistry

编辑信件的主要联系方式.
Email: brovarets@bpci.kiev.ua
乌克兰, ul. Murmanskaya 1, Kyiv, 02660


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