Synthesis of organolithium compounds from phenyl selenides

A. Krief; A. Nazih; M. Hobe

doi:10.1016/0040-4039(95)01689-F

Synthesis of organolithium compounds from phenyl selenides

A. Krief
, A. Nazih
, M. Hobe

Unite de recherche en chimie organique

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

Résumé

Alkyl aryl selenides react with lithium arenides to produce, regioselectively, alkyllithiums and lithium arylselenolates. Experimental conditions, especially the temperature, have a profound effect on the course of this reaction and on the nature of the products.

langue originale	Anglais
Pages (de - à)	8111-8114
Nombre de pages	4
journal	Tetrahedron Letters
Volume	36
Numéro de publication	44
Les DOIs	https://doi.org/10.1016/0040-4039(95)01689-F
Etat de la publication	Publié - 1 janv. 1995

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10.1016/0040-4039(95)01689-F

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@article{114000eb442a431bb94aba1302403095,

title = "Synthesis of organolithium compounds from phenyl selenides",

abstract = "Alkyl aryl selenides react with lithium arenides to produce, regioselectively, alkyllithiums and lithium arylselenolates. Experimental conditions, especially the temperature, have a profound effect on the course of this reaction and on the nature of the products.",

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

year = "1995",

month = jan,

day = "1",

doi = "10.1016/0040-4039(95)01689-F",

language = "English",

volume = "36",

pages = "8111--8114",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "44",

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TY - JOUR

T1 - Synthesis of organolithium compounds from phenyl selenides

AU - Krief, A.

AU - Nazih, A.

AU - Hobe, M.

PY - 1995/1/1

Y1 - 1995/1/1

N2 - Alkyl aryl selenides react with lithium arenides to produce, regioselectively, alkyllithiums and lithium arylselenolates. Experimental conditions, especially the temperature, have a profound effect on the course of this reaction and on the nature of the products.

AB - Alkyl aryl selenides react with lithium arenides to produce, regioselectively, alkyllithiums and lithium arylselenolates. Experimental conditions, especially the temperature, have a profound effect on the course of this reaction and on the nature of the products.

UR - https://www.scopus.com/pages/publications/0028862238

U2 - 10.1016/0040-4039(95)01689-F

DO - 10.1016/0040-4039(95)01689-F

M3 - Article

AN - SCOPUS:0028862238

SN - 0040-4039

VL - 36

SP - 8111

EP - 8114

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 44

ER -

Synthesis of organolithium compounds from phenyl selenides

Résumé

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