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Regioselective Synthesis ofFluorohydrines via SN2-Type Ring-Opening of Epoxideswith TBABF-KHF2
Akiyama, Yuriko
Fukuhara, Tsuyoshi
Hara, Shoji
?, ??
Location: http://www.thieme-chemistry.com/thieme-chemistry/journals/info/index.shtml
http://www.thieme-connect.com/ejournals/abstract/synlett/doi/10.1055/s-2003-40865
http://hdl.handle.net/2115/628
Synlett. 2003(10), 2003, 1530-1532

We found that the ring-opening fluorination of terminal epoxidesusing TBABF-KHF2 proceeds with high selectivity throughthe SN2 mechanism. As TBABF-KHF2 iseasily obtainable, is stable, and can be used in glassware, it canbe a useful reagent for 1-fluoro-2-alkanol synthesis from the terminalepoxides.

Belongs to: Hokkaido University Collection of Scholarly and Academic Papers

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Regioselective Synthesis ofFluorohydrines via SN2-Type Ring-Opening of Epoxideswith TBABF-KHF2
Id. 5707285
Idioma inglés
Titulo Regioselective Synthesis ofFluorohydrines via SN2-Type Ring-Opening of Epoxideswith TBABF-KHF2
Autor(es) Akiyama, Yuriko
Fukuhara, Tsuyoshi
Hara, Shoji
?, ??
Location http://www.thieme-chemistry.com/thieme-chemistry/journals/info/index.shtml
http://www.thieme-connect.com/ejournals/abstract/synlett/doi/10.1055/s-2003-40865
http://hdl.handle.net/2115/628
Synlett. 2003(10), 2003, 1530-1532
Versión 1.0
Estado Final
Descripción We found that the ring-opening fluorination of terminal epoxidesusing TBABF-KHF2 proceeds with high selectivity throughthe SN2 mechanism. As TBABF-KHF2 iseasily obtainable, is stable, and can be used in glassware, it canbe a useful reagent for 1-fluoro-2-alkanol synthesis from the terminalepoxides.
Tipo 43167 bytes
application/pdf
Palabras clave epoxides
Tipo de recurso article (author version)
Tipo de Interactividad Expositivo
Nivel de Interactividad muy bajo
Audiencia Estudiante
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Estructura Atomic
Coste no
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Formatos 43167 bytes
application/pdf
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Fecha de contribución 25-oct-2007
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