Lewis acid-catalyzed [3+3] annulation of donor-acceptor cyclopropanes and indonyl alcohols: one step synthesis of substituted carbazoles with promising photophysical properties

dc.contributor.author	Varshnaya, R. K.
dc.contributor.author	Banerjee, P.
dc.date.accessioned	2021-08-25T23:25:39Z
dc.date.available	2021-08-25T23:25:39Z
dc.date.issued	2021-08-26
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/2503
dc.description.abstract	A highly efficient protocol to access carbazole from donor−acceptor cyclopropane and indonyl alcohol via [3+3] annulation in the presence of a Lewis acid has been demonstrated. This method facilitates the post functionalization of the substituted carbazole into a fully conjugated π-system exhibiting intense emission bands in the visible range of the spectrum and also offers a convenient route toward the synthesis of pityriazole derivatives.	en_US
dc.language.iso	en_US	en_US
dc.title	Lewis acid-catalyzed [3+3] annulation of donor-acceptor cyclopropanes and indonyl alcohols: one step synthesis of substituted carbazoles with promising photophysical properties	en_US
dc.type	Article	en_US