Abstract
The account covers a new reaction in phosphorus chemistry, namely, the interaction of 2,2,2-trihalobenzo-1,3,2-dioxaphospholes with aryl(alkyl)acetylenes, which leads to the formation of benzo[e]-1,2-oxaphosphinine derivatives, or “phosphacoumarins.” The easy formation of a P-C bond and phosphoryl group, the ipso-substitution of the oxygen atom by the carbon one, and selective chlorination para to endocyclic oxygen are realized under mild conditions in this reaction. The ipso-substitution of a tertiary butyl group and a bromine atom also takes place in some cases.
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Published in Russian in Obzornyi Zhurnal po Khimii, 2011, Vol. 1, No. 1, pp. 29–57.
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Mironov, V.F., Nemtarev, A.V. Reaction of P,P,P-trihalogenbenzo-1,3,2-dioxaphospholes with terminal acetylenes: Phosphorus-carbon bond formation and the ipso-substitution of oxygen by carbon. Ref. J. Chem. 1, 27–55 (2011). https://doi.org/10.1134/S2079978011010067
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DOI: https://doi.org/10.1134/S2079978011010067