A Cascade Synthesis of Hetero-arylated Triarylmethanes Through a Double 5-endo-dig Cyclization Sequence

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DC Field	Value	Language
dc.contributor.author	Paluru, Dilip K.	-
dc.contributor.author	Mahesh, S.	-
dc.contributor.author	Ahmad, Feroz	-
dc.contributor.author	Anand, R.V.	-
dc.date.accessioned	2020-11-16T09:38:27Z	-
dc.date.available	2020-11-16T09:38:27Z	-
dc.date.issued	2019	-
dc.identifier.citation	Chemistry - An Asian Journal, 14(24). pp. 4688-4695.	en_US
dc.identifier.other	10.1002/asia.201900960	-
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/abs/10.1002/asia.201900960	-
dc.identifier.uri	http://hdl.handle.net/123456789/1641	-
dc.description.abstract	A sequential two‐step method for the synthesis of hetero‐arylated triarylmethanes through a Ag‐catalyzed sequential double cyclization–nucleophilic addition cascade is described. This methodology basically involves an initial 5‐endo‐dig cyclization of o‐alkynyl anilines to provide 2‐substituted indole derivatives, which then react with 2‐(2‐enynyl)‐pyridines to afford indolizine‐containing unsymmetrical triarylmethanes through another 5‐endo‐dig cyclization.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley Online Library	en_US
dc.subject	5-endo-dig Cyclization	en_US
dc.subject	Domino reactions	en_US
dc.subject	Indolizine	en_US
dc.subject	Heterocycles	en_US
dc.subject	Triarylmethanes	en_US
dc.title	A Cascade Synthesis of Hetero-arylated Triarylmethanes Through a Double 5-endo-dig Cyclization Sequence	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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