Regio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates

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Regio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates

dc.contributor.buuauthor	Coşku, Necdet
dc.contributor.department	Fen Edebiyat Fakültesi
dc.contributor.department	Kimya Bölümü
dc.date.accessioned	2021-06-30T11:20:40Z
dc.date.available	2021-06-30T11:20:40Z
dc.date.issued	1997-10-06
dc.description.abstract	Delta(3)-Imidazoline 3-oxides 1 underwent regio and diastereoselective cycloaddition with aryl isocyanates 2 to give 5,6,7,7a-tetrahydroimidazo[1,5-(b) under bar][1,2,4]oxadiazol-2(1 (H) under bar)-ones 3 in excellent yields. Thermally and chemically induced retro cycloaddition of compounds 3 was demonstrated.
dc.identifier.citation	Coşkun, N. (1997). "Regio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates". Tetrahedron, 53(40), 13873-13882.
dc.identifier.doi	10.1016/S0040-4020(97)00876-4
dc.identifier.endpage	13882
dc.identifier.issn	0040-4020
dc.identifier.issue	40
dc.identifier.scopus	2-s2.0-0037988226
dc.identifier.startpage	13873
dc.identifier.uri	https://doi.org/10.1016/S0040-4020(97)00876-4
dc.identifier.uri	https://www.sciencedirect.com/science/article/pii/S0040402097008764
dc.identifier.uri	http://hdl.handle.net/11452/20937
dc.identifier.volume	53
dc.identifier.wos	A1997XZ44700029
dc.indexed.scopus	Scopus
dc.indexed.wos	SCIE
dc.language.iso	en
dc.publisher	Pergamon-Elsevier Science Ltd
dc.relation.journal	Tetrahedron
dc.relation.publicationcategory	Makale - Uluslararası Hakemli Dergi
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject	Chemistry
dc.subject	N-oxides
dc.subject.wos	Chemistry, organic
dc.title	Regio and diastereoselective addition of imidazoline 3-oxides to aryl isocyanates
dc.type	Article
dspace.entity.type	Publication
local.contributor.department	Fen Edebiyat Fakültesi/Kimya Bölümü
local.indexed.at	WOS
local.indexed.at	Scopus