A facile access to substituted benzo[a]fluorenes from o -alkynylbenzaldehydes via in situ formed acetals

dc.contributor.author Manojveer, Seetharaman
dc.contributor.author Balamurugan, Rengarajan
dc.date.accessioned 2022-03-27T08:39:22Z
dc.date.available 2022-03-27T08:39:22Z
dc.date.issued 2014-07-31
dc.description.abstract In situ formed acetal changes the course of Brønsted acid-catalyzed reaction of ortho -alkynylbenzaldehydes with arylalkynes altogether. By utilizing this, an efficient domino approach for the regioselective synthesis of substituted benzo[a]fluorenes has been developed under mild reaction conditions. In situ formed acetal facilitates the intermolecular heteroalkyne metathesis and subsequent trans to cis isomerization of a double bond to effect the intramolecular annulation. © Partner Organisations 2014.
dc.identifier.citation Chemical Communications. v.50(69)
dc.identifier.issn 13597345
dc.identifier.uri 10.1039/c4cc03934c
dc.identifier.uri http://xlink.rsc.org/?DOI=C4CC03934C
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11383
dc.title A facile access to substituted benzo[a]fluorenes from o -alkynylbenzaldehydes via in situ formed acetals
dc.type Journal. Article
dspace.entity.type
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