Stereoselective synthesis of pyrrolo[1,2-a]indoles from allenes in PEG-400 as the reaction medium

dc.contributor.author	Phani Pavan, M.
dc.contributor.author	Kumara Swamy, K. C.
dc.date.accessioned	2022-03-27T09:51:29Z
dc.date.available	2022-03-27T09:51:29Z
dc.date.issued	2011-05-30
dc.description.abstract	Base-catalyzed domino cyclization of allenes with 3-chloro-2-formylindoles in PEG-400 was investigated. Pyrroloindoles were formed stereoselectively as single products. The structure of the product depends on the type of allene used. Two compounds have been characterized by single crystal X-ray diffraction. © Georg Thieme Verlag Stuttgart · New York.
dc.identifier.citation	Synlett
dc.identifier.issn	09365214
dc.identifier.uri	10.1055/s-0030-1260533
dc.identifier.uri	http://www.thieme-connect.de/DOI/DOI?10.1055/s-0030-1260533
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/13377
dc.subject	3-chloro-2-formylindole
dc.subject	allenes
dc.subject	domino cyclization
dc.subject	PEG-400
dc.subject	pyrroloindoles
dc.title	Stereoselective synthesis of pyrrolo[1,2-a]indoles from allenes in PEG-400 as the reaction medium
dc.type	Journal. Article
dspace.entity.type

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