The Michael Addition of Indole to α,β-Unsaturated Ketones Catalyzed by Iodine at Room Temperature

Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/95241

DC Field	Value
dc.title	The Michael Addition of Indole to α,β-Unsaturated Ketones Catalyzed by Iodine at Room Temperature
dc.contributor.author	Wang, S.-Y.
dc.contributor.author	Ji, S.-J.
dc.contributor.author	Loh, T.-P.
dc.date.accessioned	2014-10-16T08:45:28Z
dc.date.available	2014-10-16T08:45:28Z
dc.date.issued	2003
dc.identifier.citation	Wang, S.-Y.,Ji, S.-J.,Loh, T.-P. (2003). The Michael Addition of Indole to α,β-Unsaturated Ketones Catalyzed by Iodine at Room Temperature. Synlett (15) : 2377-2379. ScholarBank@NUS Repository.
dc.identifier.issn	09365214
dc.identifier.uri	http://scholarbank.nus.edu.sg/handle/10635/95241
dc.description.abstract	Indole undergoes conjugate addition with α,β-unsaturated ketones by means of alkylation of indole in the presence of a catalytic amount of molecular I2 at room temperature to afford the corresponding adduct in excellent yields (up to 96%). The substitution on the indole nucleus occurred exclusively at the 3-position. N-alkylation products have not been observed.
dc.source	Scopus
dc.subject	Indoles
dc.subject	Michael reaction
dc.subject	Molecular iodine
dc.type	Article
dc.contributor.department	CHEMISTRY
dc.description.sourcetitle	Synlett
dc.description.issue	15
dc.description.page	2377-2379
dc.description.coden	SYNLE
dc.identifier.isiut	NOT_IN_WOS
Appears in Collections:	Staff Publications

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