Synthesis of bis(4-hydroxyphenyl) selenide and epoxide and acrylate monomers on this basis Full article
Journal |
Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393 |
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Output data | Year: 2015, Volume: 51, Number: 2, Pages: 198-201 Pages count : 4 DOI: 10.1134/S1070428015020104 | ||
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Abstract:
Reaction of SeCl2 with PhOH has afforded bis(4-hydroxyphenyl) selenide, whose treatment with epichlorohydrin provides a diepoxide that is transformed in bisacrylate and further in tetraacrylate via opening of the epoxide rings with acrylic acid followed by acylation with acryloyl chloride.
Cite:
Balina S.V.
, Russkikh V.V.
, Orlova N.A.
, Ogneva L.N.
, Shelkovnikov V.V.
Synthesis of bis(4-hydroxyphenyl) selenide and epoxide and acrylate monomers on this basis
Russian Journal of Organic Chemistry. 2015. V.51. N2. P.198-201. DOI: 10.1134/S1070428015020104 WOS Scopus РИНЦ
Synthesis of bis(4-hydroxyphenyl) selenide and epoxide and acrylate monomers on this basis
Russian Journal of Organic Chemistry. 2015. V.51. N2. P.198-201. DOI: 10.1134/S1070428015020104 WOS Scopus РИНЦ
ArticleLinkType.TRANSLATED_TO_ORIGINAL:
Балина С.В.
, Русских В.В.
, Орлова Н.А.
, Огнева Л.Н.
, Шелковников В.В.
Синтез бис(4-гидроксифенил)селенида и эпоксидных и акрилатных мономеров на его основе
Журнал органической химии (RUSS J ORG CHEM+). 2015. Т.51. №2. С.210-213. РИНЦ
Синтез бис(4-гидроксифенил)селенида и эпоксидных и акрилатных мономеров на его основе
Журнал органической химии (RUSS J ORG CHEM+). 2015. Т.51. №2. С.210-213. РИНЦ
Dates:
Published print: | Feb 1, 2015 |
Published online: | Mar 26, 2015 |
Identifiers:
Web of science | WOS:000351844300010 |
Scopus | 2-s2.0-84925865870 |
Elibrary | 24020331 |
OpenAlex | W2037970128 |