Highly diastereoselective synthesis of new indolopyrroloquinolines through intramolecular imino Diels-Alder reactions

dc.contributor.author	Gaddam, Vikram
dc.contributor.author	Nagarajan, Rajagopal
dc.date.accessioned	2022-03-27T08:40:43Z
dc.date.available	2022-03-27T08:40:43Z
dc.date.issued	2007-10-08
dc.description.abstract	A new, efficient and highly diastereoselective one-pot synthesis of cis-fused indolopyrroloquinoline derivatives is described through imino Diels-Alder reaction of substituted anilines or naphthylamines with N-prenylated-2-formyl-3-chloroindoles catalyzed by La(OTf)3. © 2007 Elsevier Ltd. All rights reserved.
dc.identifier.citation	Tetrahedron Letters. v.48(41)
dc.identifier.issn	00404039
dc.identifier.uri	10.1016/j.tetlet.2007.08.016
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S0040403907015973
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/11467
dc.subject	Imino Diels-Alder reactions
dc.subject	Indolopyrroloquinoline
dc.subject	Lanthanum triflate
dc.subject	Pyrroloindole
dc.subject	Pyrroloquinoline
dc.title	Highly diastereoselective synthesis of new indolopyrroloquinolines through intramolecular imino Diels-Alder reactions
dc.type	Journal. Article
dspace.entity.type

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