Organocatalytic enantioselective synthesis of C3 functionalized indole derivatives

dc.contributor.author	Kaur, J.
dc.contributor.author	Islam, N.
dc.contributor.author	Kumar, A.
dc.contributor.author	Bhardwaj, V. K.
dc.contributor.author	Chimni, S. S.
dc.date.accessioned	2021-10-04T10:58:03Z
dc.date.available	2021-10-04T10:58:03Z
dc.date.issued	2021-10-04
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/2883
dc.description.abstract	A highly enantioselective Michael addition reaction of indolylnitroalkenes with 1,3-dicarbonyl compounds has been developed to obtain enantiomerically enriched 3-(2-nitro-1-(1-tosyl-1H-indol-3-yl) ethyl)pentane-2,4-dione derivatives in up to 98% ee using BnCPN as an organocatalyst. The transition state structure has been predicted using DFT calculation	en_US
dc.language.iso	en_US	en_US
dc.subject	Organocatalysis	en_US
dc.subject	Michael addition reaction	en_US
dc.subject	Indolylnitroalkenes	en_US
dc.subject	Enantioselective	en_US
dc.subject	DFT	en_US
dc.title	Organocatalytic enantioselective synthesis of C3 functionalized indole derivatives	en_US
dc.type	Article	en_US