Lewis acid catalyzed diastereoselective cycloaddition reactions of Donor-Acceptor cyclopropanes and vinyl azides: synthesis of functionalized azidocyclopentane and tetrahydropyridine derivatives

dc.contributor.author	Dey, R.
dc.contributor.author	Banerjee, P.
dc.date.accessioned	2021-10-11T06:35:56Z
dc.date.available	2021-10-11T06:35:56Z
dc.date.issued	2021-10-11
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/3005
dc.description.abstract	Lewis acid catalyzed [3 + 2]-cycloaddition reaction of donor−acceptor cyclopropanes with vinyl azides has been developed to obtain diastereomerically enriched azidocyclopentane derivatives. In addition, thermal chemoselective ring expansion of azidocyclopentanes to tetrahydropyridine derivatives and further diastereospecific reduction to a substituted piperidine derivative, with an excellent yield, was also achieved.	en_US
dc.language.iso	en_US	en_US
dc.title	Lewis acid catalyzed diastereoselective cycloaddition reactions of Donor-Acceptor cyclopropanes and vinyl azides: synthesis of functionalized azidocyclopentane and tetrahydropyridine derivatives	en_US
dc.type	Article	en_US