Lewis acid catalyzed formal [3+2] cycloaddition of donor-acceptor cyclopropanes and 1-Azadienes: synthesis of imine functionalized cyclopentanes and pyrrolidine derivatives

dc.contributor.author	Verma, K.
dc.contributor.author	Banerjee, P.
dc.date.accessioned	2017-12-21T11:25:00Z
dc.date.available	2017-12-21T11:25:00Z
dc.date.issued	2017-12-21
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/874
dc.description.abstract	Lewis acid catalyzed formal [3+2] cycloadditions of 1-azadienes with donor acceptor cyclopropanes to synthesize varieties of imine functionalized cyclopentanes and pyrrolidine derivatives in moderate to high yield have been developed. Moreover, pharmaceutically relevant azabicyclo[3.2.1] octane, bearing two all-carbon quaternary stereogenic centers at the bridgehead positions, has been synthesized by nosyl group deprotection and intramolecular amidation of imine functionalized cyclopentane derivative.	en_US
dc.language.iso	en_US	en_US
dc.subject	Donor-Acceptor Cyclopropane	en_US
dc.subject	1-Azadienes	en_US
dc.subject	Imine Functionalized Cyclopentanes	en_US
dc.subject	Pyrrolidine	en_US
dc.subject	azabicyclo[3.2.1]octane	en_US
dc.title	Lewis acid catalyzed formal [3+2] cycloaddition of donor-acceptor cyclopropanes and 1-Azadienes: synthesis of imine functionalized cyclopentanes and pyrrolidine derivatives	en_US
dc.type	Article	en_US