Catalyst-Free One-Pot Tandem Reduction of Oxo and Ene/Yne Functionalities by Hydrazine: Synthesis of Substituted Oxindoles from Isatins

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DC Field	Value	Language
dc.contributor.author	Jha, Anil	-
dc.date.accessioned	2021-10-17T13:58:16Z	-
dc.date.available	2021-10-17T13:58:16Z	-
dc.date.issued	2014-04-15	-
dc.identifier.uri	https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201402038	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2883	-
dc.description.abstract	An unprecedented hydrazine-mediated tandem reduction of oxo and N-ene/yne functionalities of substituted isatins is reported to access various oxindoles. The reaction is performed by treating N-(2-alkenyl)/propargylisatins with hydrazine hydrate under catalyst-free refluxing conditions. The reduction proceeds efficiently without the aid of any catalyst at ambient pressure.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Chemistry	en_US
dc.subject	Catalyst-Free	en_US
dc.subject	Synthesis	en_US
dc.subject	Oxindoles	en_US
dc.title	Catalyst-Free One-Pot Tandem Reduction of Oxo and Ene/Yne Functionalities by Hydrazine: Synthesis of Substituted Oxindoles from Isatins	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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