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Studies on the catalysis of the reaction of organotin phenoxides with bis(2,2,2‐trichloroethyl) azodicarboxylate by lithium perchlorate
Author(s) -
Kinart Wojciech J.,
Kinart Cezary M.,
Tran Quang T.,
Oszczȩda Rafał,
Nazarski Ryszard B.
Publication year - 2004
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.681
Subject(s) - chemistry , phenols , perchlorate , lithium (medication) , lithium perchlorate , catalysis , phenol , organic chemistry , ion , medicine , electrode , electrochemistry , endocrinology
Organotin phenoxides, which are distinctly more active than the corresponding phenols, react at room temperature with bis(2,2,2‐trichloroethyl) azodicarboxylate to produce para‐substituted phenolic hydrazides in high yields. Copyright © 2004 John Wiley & Sons, Ltd.
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