Molecules (Jul 2015)

Synthesis of Oxygen Heterocycles via Aromatic C-O Bond Formation Using Arynes

  • Hideto Miyabe

DOI
https://doi.org/10.3390/molecules200712558
Journal volume & issue
Vol. 20, no. 7
pp. 12558 – 12575

Abstract

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Most of the synthetic approaches to the benzo-fused heterocycles containing an oxygen atom have involved the use of phenol derivatives as a starting material. This review highlights the new synthetic approaches involving the aromatic C-O bond-forming process using arynes. The insertion of arynes into the C=O bond gives the unstable intermediates, [2 + 2] cycloaddition-type adducts, which can be easily converted into a variety of oxygen atom-containing heterocycles in a single operation. In this review, the syntheses of oxygen heterocycles, such as coumarin, chromene, xanthene, dihydrobenzofuran and benzofuran derivatives, via the insertion of arynes into the C=O bond of aldehydes or formamides are summarized.

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