Substituted benzaldehydes in the darzens condensation with alkyl dihaloacetates

dc.contributor.author	Mamedov V.
dc.contributor.author	Berdnikov E.
dc.contributor.author	Tsuboi S.
dc.contributor.author	Hamamoto H.
dc.contributor.author	Komiyama T.
dc.contributor.author	Gorbunova E.
dc.contributor.author	Gubaidullin A.
dc.contributor.author	Litvinov I.
dc.date.accessioned	2018-09-18T20:17:27Z
dc.date.available	2018-09-18T20:17:27Z
dc.date.issued	2006
dc.identifier.issn	1066-5285
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/138360
dc.description.abstract	The Darzens reaction of dihaloacetic acid esters with aromatic aldehydes produces either arylhaloglycidic or arylhalopyruvic esters depending on the nature of the substituent in the aromatic ring. Alkyl p- methoxyphenylchloropyruvates undergo spontaneous intermolecular cyclocondensation to form pyranone or furanone derivatives depending on the character of the alkyl fragment. © 2006 Springer Science+Business Media, Inc.
dc.relation.ispartofseries	Russian Chemical Bulletin
dc.subject	Benzaldehydes
dc.subject	Darzens reaction
dc.subject	Dihaloacetic acids
dc.subject	Epoxides
dc.subject	Furan-2-ones
dc.subject	Glycidic acids
dc.subject	Pyran-2,3-diones
dc.subject	Pyruvic acids
dc.subject	X-ray diffraction study
dc.title	Substituted benzaldehydes in the darzens condensation with alkyl dihaloacetates
dc.type	Article
dc.relation.ispartofseries-issue	8
dc.relation.ispartofseries-volume	55
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1455
dc.source.id	SCOPUS10665285-2006-55-8-SID33845945757

Файлы в этом документе

Размер: 43.75Kb

Формат: PDF

Публикации сотрудников КФУ Scopus [24551]
Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.