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A facile access to substituted benzo[a]fluorenes from o-alkynylbenzaldehydes via in situ formed acetals†
Seetharaman Manojveer,Rengarajan Balamurugan
Chemical Communications Pub Date : 07/08/2014 00:00:00 , DOI:10.1039/C4CC03934C
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.

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