Efficient, Stereoselective Approach to the Synthesis of 3-(1-Phenyl-2-(Z-styrylsulfonyl)-1H-imidazol-4-yl)-2H-chromen-2-ones

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DC Field	Value	Language
dc.contributor.author	Guravaiah, N.	-
dc.contributor.author	Rao, V.R.	-
dc.date.accessioned	2025-02-06T06:14:00Z	-
dc.date.available	2025-02-06T06:14:00Z	-
dc.date.issued	2011	-
dc.identifier.citation	10.1080/00397911003797874	en_US
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/3155	-
dc.description	NITW	en_US
dc.description.abstract	Reaction of phenyl acetylene with 3-(1-aryl-2-mercapto-4-imidazolyl)-2H-1-benzopyran-2-ones (4) in the presence of sodium hydroxide in absolute ethanol led to the formation of 3-(1-phenyl-2-(Z-styrylthio)-1H-imidazol-4-yl)-2H-chromen-2-ones (6) in excellent yields. These, on further oxidation with H2O2/AcOH, gave the corresponding sulfones (7) with retention of stereochemistry.	en_US
dc.language.iso	en	en_US
dc.publisher	Synthetic Communications An International Journal for Rapid Communication of Synthetic Organic	en_US
dc.subject	3-(2-Mercapto-1-phenyl-1H-imidazol-4-yl)-2H-chromen-2-ones	en_US
dc.subject	phenylacetylene	en_US
dc.title	Efficient, Stereoselective Approach to the Synthesis of 3-(1-Phenyl-2-(Z-styrylsulfonyl)-1H-imidazol-4-yl)-2H-chromen-2-ones	en_US
dc.type	Article	en_US
Appears in Collections:	Chemistry

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