Synthesis of 1,2,4-Trisubstituted-(1H)‑imidazoles through Cu(OTf)2‑/ I2‑Catalyzed C−C Bond Cleavage of Chalcones and Benzylamines

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DC Field	Value	Language
dc.contributor.author	Salfeena, C T F	-
dc.contributor.author	Renjitha, J	-
dc.contributor.author	Davis, R	-
dc.contributor.author	Suresh, E	-
dc.contributor.author	Sasidhar, B S	-
dc.date.accessioned	2018-08-21T06:52:57Z	-
dc.date.available	2018-08-21T06:52:57Z	-
dc.date.issued	2018-07	-
dc.identifier.citation	ACS Omega, 3(7):8074–8082	en_US
dc.identifier.uri	http://10.10.100.66:8080/xmlui/handle/123456789/3261	-
dc.description.abstract	1,2,4-Trisubstituted-(1H)-imidazoles have been synthesized by the Cu(OTf)2- and I2-catalyzed unusual C−C bond cleavage of chalcones and benzylamines. After the α,β-unsaturated C−C bond cleavage, the β-portion is eliminated from the reaction. Various aryl- and heteroarylsubstituted chalcones and benzylamines were well tolerated in this unusual transformation to yield the trisubstituted-(1H)-imidazoles.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.title	Synthesis of 1,2,4-Trisubstituted-(1H)‑imidazoles through Cu(OTf)2‑/ I2‑Catalyzed C−C Bond Cleavage of Chalcones and Benzylamines	en_US
dc.type	Article	en_US
Appears in Collections:	2018

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