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

A. Krief, M. Hobe

Research output: Contribution to journalArticle

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'.
Original languageEnglish
Pages (from-to)6529-6532
Number of pages4
JournalTetrahedron Letters
Volume33
Issue number43
DOIs
Publication statusPublished - 1 Jan 1992

Fingerprint

Cyclopropanes
Tin
Catalytic Domain
Derivatives
n-butyllithium

Cite this

@article{e273bcb3aef7455caf61b43aff82903f,
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",
day = "1",
doi = "10.1016/S0040-4039(00)79034-4",
language = "English",
volume = "33",
pages = "6529--6532",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "43",

}

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

In: Tetrahedron Letters, Vol. 33, No. 43, 01.01.1992, p. 6529-6532.

Research output: Contribution to journalArticle

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.

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'.

UR - http://www.scopus.com/inward/record.url?scp=0026674162&partnerID=8YFLogxK

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

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

M3 - Article

AN - SCOPUS:0026674162

VL - 33

SP - 6529

EP - 6532

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 43

ER -