Asymmetric epoxidation of fujorinated allylic alcohols

C. Gosmini; T. Dubuffet; R. Sauvêtre; J. F. Normant

doi:10.1016/S0957-4166(00)82361-7

Asymmetric epoxidation of fujorinated allylic alcohols

C. Gosmini
, T. Dubuffet
, R. Sauvêtre
, J. F. Normant

Laboratoire de Chimie des Organoélémentsniversité P. et M. Curie Tour

Résultats de recherche: Contribution à un journal › Article › Revue par des pairs

12 Citations (Scopus)

Résumé

The asymmetric epoxidation of an α,β-difluoro primary allylic alcohol, and of two α-fluoro secondary allylic alcohols follows the pattern known with non fluorinated analogs. The fluoro epoxides thus formed can be transformed into chiral α-ketols and into an α-fluoroacid.

langue originale	Anglais
Pages (de - à)	223-230
Nombre de pages	8
journal	Tetrahedron Asymmetry
Volume	2
Numéro de publication	3
Les DOIs	https://doi.org/10.1016/S0957-4166(00)82361-7
état	Publié - 1 janv. 1991
Modification externe	Oui

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10.1016/S0957-4166(00)82361-7

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title = "Asymmetric epoxidation of fujorinated allylic alcohols",

abstract = "The asymmetric epoxidation of an α,β-difluoro primary allylic alcohol, and of two α-fluoro secondary allylic alcohols follows the pattern known with non fluorinated analogs. The fluoro epoxides thus formed can be transformed into chiral α-ketols and into an α-fluoroacid.",

author = "C. Gosmini and T. Dubuffet and R. Sauv{\^e}tre and Normant, \{J. F.\}",

year = "1991",

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doi = "10.1016/S0957-4166(00)82361-7",

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T1 - Asymmetric epoxidation of fujorinated allylic alcohols

AU - Gosmini, C.

AU - Dubuffet, T.

AU - Sauvêtre, R.

AU - Normant, J. F.

PY - 1991/1/1

Y1 - 1991/1/1

N2 - The asymmetric epoxidation of an α,β-difluoro primary allylic alcohol, and of two α-fluoro secondary allylic alcohols follows the pattern known with non fluorinated analogs. The fluoro epoxides thus formed can be transformed into chiral α-ketols and into an α-fluoroacid.

AB - The asymmetric epoxidation of an α,β-difluoro primary allylic alcohol, and of two α-fluoro secondary allylic alcohols follows the pattern known with non fluorinated analogs. The fluoro epoxides thus formed can be transformed into chiral α-ketols and into an α-fluoroacid.

U2 - 10.1016/S0957-4166(00)82361-7

DO - 10.1016/S0957-4166(00)82361-7

M3 - Article

AN - SCOPUS:0025907469

SN - 0957-4166

VL - 2

SP - 223

EP - 230

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

IS - 3

ER -

Asymmetric epoxidation of fujorinated allylic alcohols

Résumé

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