Highly diastereoselective synthesis of new chromenylaminoanthraquinones through a one-pot, three-component hetero Diels-Alder reaction

dc.contributor.author	Gaddam, Vikram
dc.contributor.author	Sreenivas, Devanga K.
dc.contributor.author	Nagarajan, Rajagopal
dc.date.accessioned	2022-03-27T08:40:49Z
dc.date.available	2022-03-27T08:40:49Z
dc.date.issued	2006-12-25
dc.description.abstract	A new, efficient, and diastereoselective one-pot synthesis of cis-fused pyrano and furano chromenylaminoanthraquinones through hetero Diels-Alder reaction of 1-aminoanthraquinone and salicylaldehydes with electron-rich alkenes such as 3,4-dihydro-2H-pyran, 2,3-dihydrofuran, and ethyl vinyl ether under mild conditions is reported. © 2006 Elsevier Ltd. All rights reserved.
dc.identifier.citation	Tetrahedron Letters. v.47(52)
dc.identifier.issn	00404039
dc.identifier.uri	10.1016/j.tetlet.2006.10.104
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S0040403906021307
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/11472
dc.subject	Aminoanthraquinone
dc.subject	Arylaminochromenes
dc.subject	Chromenylaminoanthraquinones
dc.subject	Cycloaddition
dc.subject	Electron-rich alkenes
dc.title	Highly diastereoselective synthesis of new chromenylaminoanthraquinones through a one-pot, three-component hetero Diels-Alder reaction
dc.type	Journal. Article
dspace.entity.type

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