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

A. Krief, M. Hobe

Résultats de recherche: Contribution à un journal/une revueArticle

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 originaleAnglais
Pages (de - à)6529-6532
Nombre de pages4
journalTetrahedron Letters
Volume33
Numéro de publication43
Les DOIs
étatPublié - 1 janv. 1992

Empreinte digitale

Cyclopropanes
Tin
Catalytic Domain
Derivatives
n-butyllithium

Citer ceci

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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 = "1",
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On the mechanism of the synthesis of aryl cyclopropanes from γ-benzenesulfonyloxyalkyl seleno and tin derivatives and n-butyllithium. / Krief, A.; Hobe, M.

Dans: Tetrahedron Letters, Vol 33, Numéro 43, 01.01.1992, p. 6529-6532.

Résultats de recherche: Contribution à un journal/une revueArticle

TY - JOUR

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.

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

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JO - Tetrahedron Letters

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