Synthetic routes to cyclopropylidenecarbinols and to cyclopropylidienes

S. Halazy; A. Krief

Synthetic routes to cyclopropylidenecarbinols and to cyclopropylidienes

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

Résumé

Functionalized alkylidine cyclopropanes have beeen prepared from 1-seleno 1-vinyl cyclopropanes using [2,3] sigmatropic rearrangement of their corresponding selenonium ylides. A comparison with sulphur analogues is presented.

langue originale	Anglais
Pages (de - à)	2135-2138
Nombre de pages	4
journal	Tetrahedron Letters
Volume	22
Numéro de publication	22
Etat de la publication	Publié - 1 janv. 1981

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title = "Synthetic routes to cyclopropylidenecarbinols and to cyclopropylidienes",

abstract = "Functionalized alkylidine cyclopropanes have beeen prepared from 1-seleno 1-vinyl cyclopropanes using [2,3] sigmatropic rearrangement of their corresponding selenonium ylides. A comparison with sulphur analogues is presented.",

author = "S. Halazy and A. Krief",

year = "1981",

month = jan,

day = "1",

language = "English",

volume = "22",

pages = "2135--2138",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "22",

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TY - JOUR

T1 - Synthetic routes to cyclopropylidenecarbinols and to cyclopropylidienes

AU - Halazy, S.

AU - Krief, A.

PY - 1981/1/1

Y1 - 1981/1/1

N2 - Functionalized alkylidine cyclopropanes have beeen prepared from 1-seleno 1-vinyl cyclopropanes using [2,3] sigmatropic rearrangement of their corresponding selenonium ylides. A comparison with sulphur analogues is presented.

AB - Functionalized alkylidine cyclopropanes have beeen prepared from 1-seleno 1-vinyl cyclopropanes using [2,3] sigmatropic rearrangement of their corresponding selenonium ylides. A comparison with sulphur analogues is presented.

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M3 - Article

AN - SCOPUS:0000390423

SN - 0040-4039

VL - 22

SP - 2135

EP - 2138

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 22

ER -

Synthetic routes to cyclopropylidenecarbinols and to cyclopropylidienes

Résumé

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