Reaction of Huisgen zwitterion with 1,2-benzoquinones and isatins: Expeditious synthesis of dihydro-1,2,3-benzoxadiazoles and spirooxadiazolines

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DC Field	Value	Language
dc.contributor.author	Vijay Nair, G	-
dc.contributor.author	Biju, A T	-
dc.contributor.author	Vinod, A U	-
dc.contributor.author	Suresh, E	-
dc.date.accessioned	2021-02-08T12:07:50Z	-
dc.date.available	2021-02-08T12:07:50Z	-
dc.date.issued	2005	-
dc.identifier.citation	Organic Letters 7(23):5139-5142; 10 Nov 2005	en_US
dc.identifier.issn	1523-7060	-
dc.identifier.uri	http://hdl.handle.net/123456789/3663	-
dc.description.abstract	The zwitterionic intermediate generated from dialkyl azodicarboxylate and triphenylphosphine on reaction with 3-methoxy-1,2-benzoquinones afforded dihydro-1,2,3-benzoxadiazoles. N-Substituted isatins furnished spirooxadiazolines under similar conditions.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Huisgen zwitterion	en_US
dc.subject	1,2-benzoquinones	en_US
dc.subject	Isatins	en_US
dc.subject	Dihydro-1,2,3-benzoxadiazoles	en_US
dc.subject	Spirooxadiazolines	en_US
dc.title	Reaction of Huisgen zwitterion with 1,2-benzoquinones and isatins: Expeditious synthesis of dihydro-1,2,3-benzoxadiazoles and spirooxadiazolines	en_US
dc.type	Article	en_US
Appears in Collections:	2005

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