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Regioselective Ring Opening of Epoxides with Lithium Azide
Home
Publications
Regioselective Ring Opening of Epoxides with Lithium Azide
Regioselective Ring Opening of Epoxides with Lithium Azide
AG
A. Guy
A. Guy
JD
J. Doussot
J. Doussot
CF
C. Ferroud
C. Ferroud
RG
R. Garreau
R. Garreau
AG
A. Godefroy-Falguieres
A. Godefroy-Falguieres
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1 January 1992
journal article
research article
Published by
Georg Thieme Verlag KG
in
Synthesis
Vol. 1992
(09)
,
821-822
https://doi.org/10.1055/s-1992-26233
Abstract
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.
Keywords
BENZYLIC
AZIDE/HEXAMETHYLPHOSPHORAMIDE
ARYL
SUBSTITUTED
PHENYLOXIRANE
AZIDOETHANOL
ATTACK
REGIOSELECTIVE
OPENING OF EPOXIDES
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Cited by 22 articles