Additional cycle formation from 2-dialkoxyphosphonylmethylthiazole

dc.contributor.author	Baimashev B.
dc.contributor.author	Polezhaeva N.
dc.contributor.author	Klimovitskii E.
dc.date.accessioned	2018-09-17T21:02:04Z
dc.date.available	2018-09-17T21:02:04Z
dc.date.issued	1998
dc.identifier.issn	1042-6507
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/134426
dc.description.abstract	Diisopropoxyphosphonyl-2-(4-methylthiazolyl)methane I reacts with carbonyl and α-halocarbonyl compounds by three routes. In the case of Knoevenagel or Horner-Wadsworth-Emmons reactions the corresponding ethylenes were produced, whereas employing α-halocarbonyls as partners resulted in pyrrolo[2.1b]thiazoles. 1-Phosphonyl-1-(2-thiazolyl)-ethylene undergoes smoothly [4+2] and [3+2] cycloaddition reactions.
dc.relation.ispartofseries	Phosphorus, Sulfur and Silicon and Related Elements
dc.subject	1-phosphonyl-1-thiazolylethylenes
dc.subject	3-methoxycarbonyl-5-dialkoxyphosphonyl-5-(4-methylthizol-2-yl)-2-pyrazoline
dc.subject	6-dialkoxyphosphonylpyrrolo[2.1b]thiazoles
dc.subject	Dialkoxyphosphonyl-2-(4-methylthiazolyl)methanes
dc.title	Additional cycle formation from 2-dialkoxyphosphonylmethylthiazole
dc.type	Article
dc.relation.ispartofseries-volume	132
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	251
dc.source.id	SCOPUS10426507-1998-132-SID0032236021

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