Synthesis of indenopyridine derivatives via MgI2-promoted [2+4] cycloaddition reaction of In-situ generated 2- styrylmalonate from donor-acceptor cyclopropanes and chalconimines

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DC Field	Value	Language
dc.contributor.author	Verma, K.	-
dc.contributor.author	Banerjee, P.	-
dc.date.accessioned	2018-12-28T08:37:38Z	-
dc.date.available	2018-12-28T08:37:38Z	-
dc.date.issued	2018-12-28	-
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/1107	-
dc.description.abstract	An unexpected MgI2-promoted [2+4] cycloaddition reaction of in-situ generated 2-styrylmalonate from donor-acceptor cyclopropanes with chalconimines to synthesize highly substituted indenopyridine derivatives under the mild reaction conditions have been developed. Additionally, these derivatives were utilized for the synthesis of highly substituted 9-membered lactam by oxidative C=C bond cleavage and spiro [oxoindane-pyrrolidine] derivative via Meinwald type rearrangement.	en_US
dc.language.iso	en_US	en_US
dc.subject	2-styrylmalonate	en_US
dc.subject	Donor-acceptor cyclopropanes	en_US
dc.subject	Indenopyridine	en_US
dc.subject	Chalconimines	en_US
dc.title	Synthesis of indenopyridine derivatives via MgI2-promoted [2+4] cycloaddition reaction of In-situ generated 2- styrylmalonate from donor-acceptor cyclopropanes and chalconimines	en_US
dc.type	Article	en_US
Appears in Collections:	Year-2018

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