Synthesis and resolution of the planar chirality of ester-functionalised phospharuthenocenes

Duncan Carmichael; Jürgen Klankermayer; Louis Ricard; Nicolas Seeboth

doi:10.1039/b401088d

Synthesis and resolution of the planar chirality of ester-functionalised phospharuthenocenes

Duncan Carmichael
, Jürgen Klankermayer
, Louis Ricard
, Nicolas Seeboth

CNRS
CNRS UMR 7653

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

29 Citations (Scopus)

Résumé

Menthyl phospholide ester anions provide an operationally simple and high yielding entry to the first planar chiral enantiopure phospharuthenocene derivatives.

langue originale	Anglais
Pages (de - à)	1144-1145
Nombre de pages	2
journal	Chemical Communications
Volume	4
Numéro de publication	9
Les DOIs	https://doi.org/10.1039/b401088d
état	Publié - 1 janv. 2004
Modification externe	Oui

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10.1039/b401088d

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title = "Synthesis and resolution of the planar chirality of ester-functionalised phospharuthenocenes",

abstract = "Menthyl phospholide ester anions provide an operationally simple and high yielding entry to the first planar chiral enantiopure phospharuthenocene derivatives.",

author = "Duncan Carmichael and J{\"u}rgen Klankermayer and Louis Ricard and Nicolas Seeboth",

year = "2004",

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AU - Carmichael, Duncan

AU - Klankermayer, Jürgen

AU - Ricard, Louis

AU - Seeboth, Nicolas

PY - 2004/1/1

Y1 - 2004/1/1

N2 - Menthyl phospholide ester anions provide an operationally simple and high yielding entry to the first planar chiral enantiopure phospharuthenocene derivatives.

AB - Menthyl phospholide ester anions provide an operationally simple and high yielding entry to the first planar chiral enantiopure phospharuthenocene derivatives.

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DO - 10.1039/b401088d

M3 - Article

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JO - Chemical Communications

JF - Chemical Communications

IS - 9

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Synthesis and resolution of the planar chirality of ester-functionalised phospharuthenocenes

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