The hydrogenation of β-hydroxy-γfluoro-γ-ethylenic esters as an efficient approach to the fluorohydrin substructure

Karine Lucet-Levannier; Jean Paul Lellouche; Charles Mioskowski; Florence Schneider; Claude Cassagne

doi:10.1016/0040-4039(96)00174-8

The hydrogenation of β-hydroxy-γfluoro-γ-ethylenic esters as an efficient approach to the fluorohydrin substructure

Karine Lucet-Levannier
, Jean Paul Lellouche
, Charles Mioskowski
, Florence Schneider
, Claude Cassagne

Research output: Contribution to journal › Article › peer-review

4 Scopus citations

Abstract

A novel high-yielding preparation of the fluorohydrin moiety is depicted based on the reductive hydrogenation of β-hydroxy-γ-fluoro-γ-ethylenic esters. Several useful homogeneous as well heterogeneous conditions are disclosed and discussed in this communication.

Original language	English
Pages (from-to)	2007-2010
Number of pages	4
Journal	Tetrahedron Letters
Volume	37
Issue number	12
DOIs	https://doi.org/10.1016/0040-4039(96)00174-8
State	Published - 18 Mar 1996
Externally published	Yes

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10.1016/0040-4039(96)00174-8

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title = "The hydrogenation of β-hydroxy-γfluoro-γ-ethylenic esters as an efficient approach to the fluorohydrin substructure",

abstract = "A novel high-yielding preparation of the fluorohydrin moiety is depicted based on the reductive hydrogenation of β-hydroxy-γ-fluoro-γ-ethylenic esters. Several useful homogeneous as well heterogeneous conditions are disclosed and discussed in this communication.",

author = "Karine Lucet-Levannier and Lellouche, \{Jean Paul\} and Charles Mioskowski and Florence Schneider and Claude Cassagne",

year = "1996",

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T1 - The hydrogenation of β-hydroxy-γfluoro-γ-ethylenic esters as an efficient approach to the fluorohydrin substructure

AU - Lucet-Levannier, Karine

AU - Lellouche, Jean Paul

AU - Mioskowski, Charles

AU - Schneider, Florence

AU - Cassagne, Claude

PY - 1996/3/18

Y1 - 1996/3/18

N2 - A novel high-yielding preparation of the fluorohydrin moiety is depicted based on the reductive hydrogenation of β-hydroxy-γ-fluoro-γ-ethylenic esters. Several useful homogeneous as well heterogeneous conditions are disclosed and discussed in this communication.

AB - A novel high-yielding preparation of the fluorohydrin moiety is depicted based on the reductive hydrogenation of β-hydroxy-γ-fluoro-γ-ethylenic esters. Several useful homogeneous as well heterogeneous conditions are disclosed and discussed in this communication.

UR - https://www.scopus.com/pages/publications/0029874339

U2 - 10.1016/0040-4039(96)00174-8

DO - 10.1016/0040-4039(96)00174-8

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AN - SCOPUS:0029874339

SN - 0040-4039

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EP - 2010

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 12

ER -

The hydrogenation of β-hydroxy-γfluoro-γ-ethylenic esters as an efficient approach to the fluorohydrin substructure

Abstract

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