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- W2910098511 abstract "Herein, a two-step procedure for the preparation of oxygenated ortho-methylbenzaldehyde derivatives, starting from commercially available bromoarenes, is described. The synthesis features the simultaneous and highly regioselective installation of both the methyl and the formyl group onto the benzene core via benzyne [2+2] cycloadditions with acetaldehyde lithium enolate to give the corresponding benzocyclobutenols in high yields. Bond-selective ring opening of the benzocyclobutenols under basic conditions in methanol delivers the title compounds." @default.
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- W2910098511 date "2018-12-19" @default.
- W2910098511 modified "2023-09-29" @default.
- W2910098511 title "Synthesis of Oxygenated ortho-Methylbenzaldehydes via Aryne [2+2] Cycloaddition and Benzocyclobutenol Ring Opening" @default.
- W2910098511 doi "https://doi.org/10.2533/chimia.2018.870" @default.
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