Convenient Synthesis of 3,5-Disubstituted N-Salicylidene-4-allyloxyanilines Full article
Journal |
Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393 |
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Output data | Year: 2010, Volume: 46, Number: 12, Pages: 1888-1890 Pages count : 3 DOI: 10.1134/S1070428010120195 | ||||
Tags | Schiff Base; Allyl Bromide; Anhydrous Potassium Carbonate; Salicylidene; Convenient Synthesis | ||||
Authors |
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Abstract:
We now propose a more convenient alternative procedure for the synthesis of Schiff bases from p-aminophenol in
a smaller number of steps.
Cite:
Oleinik I.I.
, Oleinik I.V.
, Ivanchev S.S.
, Tolstikov G.A.
Convenient Synthesis of 3,5-Disubstituted N-Salicylidene-4-allyloxyanilines
Russian Journal of Organic Chemistry. 2010. V.46. N12. P.1888-1890. DOI: 10.1134/S1070428010120195 WOS Scopus РИНЦ
Convenient Synthesis of 3,5-Disubstituted N-Salicylidene-4-allyloxyanilines
Russian Journal of Organic Chemistry. 2010. V.46. N12. P.1888-1890. DOI: 10.1134/S1070428010120195 WOS Scopus РИНЦ
ArticleLinkType.TRANSLATED_TO_ORIGINAL:
Олейник И.И.
, Олейник И.В.
, Иванчев С.С.
, Толстиков Г.А.
Удобный способ синтеза 3, 5-дизамещенных N-салицилиден-4-аллилоксианилинов
Журнал органической химии. 2010. Т.46. №12. С.1873-1875.
Удобный способ синтеза 3, 5-дизамещенных N-салицилиден-4-аллилоксианилинов
Журнал органической химии. 2010. Т.46. №12. С.1873-1875.
Dates:
Submitted: | Jun 3, 2009 |
Published print: | Dec 1, 2010 |
Published online: | Feb 5, 2011 |
Identifiers:
Web of science | WOS:000286985900019 |
Scopus | 2-s2.0-79951507701 |
Elibrary | 16698869 |
Chemical Abstracts | 2011:154123 |
Chemical Abstracts (print) | 154:310284 |
OpenAlex | W2052251248 |
publication.block.citing_info:
БД | Цитирований |
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OpenAlex | 1 |