On the mechanism of the synthesis of aryl cyclopropanes from γ-benzenesulfonyloxyalkyl seleno and tin derivatives and n-butyllithium

A. Krief; M. Hobe

doi:10.1016/S0040-4039(00)79034-4

On the mechanism of the synthesis of aryl cyclopropanes from γ-benzenesulfonyloxyalkyl seleno and tin derivatives and n-butyllithium

A. Krief, M. Hobe

Unite de recherche en chimie organique

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

Résumé

γ-Benzenesulfonyloxyalkyl selenides react with n-butyllithium and stereospecifically lead to aryl cyclopropanes with inversion of configuration at each of the reactive sites which is compatible with the 'W mechanism'.

langue originale	Anglais
Pages (de - à)	6529-6532
Nombre de pages	4
journal	Tetrahedron Letters
Volume	33
Numéro de publication	43
Les DOIs	https://doi.org/10.1016/S0040-4039(00)79034-4
Etat de la publication	Publié - 1 janv. 1992

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10.1016/S0040-4039(00)79034-4

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title = "On the mechanism of the synthesis of aryl cyclopropanes from γ-benzenesulfonyloxyalkyl seleno and tin derivatives and n-butyllithium",

abstract = "γ-Benzenesulfonyloxyalkyl selenides react with n-butyllithium and stereospecifically lead to aryl cyclopropanes with inversion of configuration at each of the reactive sites which is compatible with the 'W mechanism'.",

author = "A. Krief and M. Hobe",

year = "1992",

month = jan,

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doi = "10.1016/S0040-4039(00)79034-4",

language = "English",

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journal = "Tetrahedron Letters",

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T1 - On the mechanism of the synthesis of aryl cyclopropanes from γ-benzenesulfonyloxyalkyl seleno and tin derivatives and n-butyllithium

AU - Krief, A.

AU - Hobe, M.

PY - 1992/1/1

Y1 - 1992/1/1

N2 - γ-Benzenesulfonyloxyalkyl selenides react with n-butyllithium and stereospecifically lead to aryl cyclopropanes with inversion of configuration at each of the reactive sites which is compatible with the 'W mechanism'.

AB - γ-Benzenesulfonyloxyalkyl selenides react with n-butyllithium and stereospecifically lead to aryl cyclopropanes with inversion of configuration at each of the reactive sites which is compatible with the 'W mechanism'.

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U2 - 10.1016/S0040-4039(00)79034-4

DO - 10.1016/S0040-4039(00)79034-4

M3 - Article

AN - SCOPUS:0026674162

SN - 0040-4039

VL - 33

SP - 6529

EP - 6532

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 43

ER -

On the mechanism of the synthesis of aryl cyclopropanes from γ-benzenesulfonyloxyalkyl seleno and tin derivatives and n-butyllithium

Résumé

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