Regioselective ring opening of epoxides with lithium azide

DOI: 10.1055/s-1992-26233

Source and publish data:

Synthesis p. 821 - 822 (1992)

Update date:2022-08-03

Topics:

Authors:

Guy Guy

Doussot Doussot

Ferroud Ferroud

Garreau Garreau

Godefroy-Falguieres

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Article abstract of DOI:10.1055/s-1992-26233

Regioselective ring opening of substituted phenyloxirane was achieved with lithium azide/hexamethylphosphoramide by attack of azide at the non-benzylic position of the epoxide, leading to 1-aryl-2-azidoethanol.

Full text of DOI:10.1055/s-1992-26233

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Product name:2-(2,4-Dimethoxy-phenyl)-oxirane

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