Dienaminodiones, New Push-Pull Alkenes, from 3,4-DihydroxySalicylaldehyde-Derived Schiff Base

dc.contributor.author	Ravindran, J
dc.contributor.author	Ingaladal, N
dc.contributor.author	Lankalapalli, RS
dc.date.accessioned	2021-05-14T06:59:18Z
dc.date.available	2021-05-14T06:59:18Z
dc.date.issued	2020-11
dc.identifier.citation	Tetrahedron Letters;61(46):152531.	en_US
dc.identifier.uri	https://doi.org/10.1016/j.tetlet.2020.152531
dc.identifier.uri	http://hdl.handle.net/123456789/3765
dc.description.abstract	An atom-economical one-pot synthesis of a new push-pull dienaminodiones from a 3,4-dihydroxysalicylaldehyde-derived Schiff base and indoles in the presence of phenyliodine(III) diacetate is described. Variation of indoles and anilines constitute a broad substrate scope of the methodology with good to moderate yields. Formation of Schiff base followed by an indole addition to afford dienaminodione takes place in one-pot; thus, the present method serves as a sequential multicomponent reaction. The present work also serves as a methodology to afford indole variants of natural product talaroenamine B.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsevier	en_US
dc.subject	dienaminone	en_US
dc.subject	push-pull effect	en_US
dc.subject	one-pot synthesis	en_US
dc.subject	talaroenamine	en_US
dc.subject	oxidative transformation	en_US
dc.subject	N-salicylideneaniline Schiff base	en_US
dc.title	Dienaminodiones, New Push-Pull Alkenes, from 3,4-DihydroxySalicylaldehyde-Derived Schiff Base	en_US
dc.type	Article	en_US