Synthesis and Diels-Alder reactions of allylidenecyclopropane [4]

F. Zutterman; A. Krief

Synthesis and Diels-Alder reactions of allylidenecyclopropane [4]

F. Zutterman, A. Krief

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

Résumé

Allylidenecyclopropane, readily available from 1-lithio-1-(phenylthio)cyclopropane, reacts with a large variety of electrophilic olefins and produces functionalized spirooctenes. The reactions are, in most cases, highly regioselective but lead mainly to the unexpected regioisomers.

langue originale	Anglais
Pages (de - à)	1135-1137
Nombre de pages	3
journal	Journal of Organic Chemistry
Volume	48
Numéro de publication	7
Etat de la publication	Publié - 1 janv. 1983

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Contient cette citation

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title = "Synthesis and Diels-Alder reactions of allylidenecyclopropane [4]",

abstract = "Allylidenecyclopropane, readily available from 1-lithio-1-(phenylthio)cyclopropane, reacts with a large variety of electrophilic olefins and produces functionalized spirooctenes. The reactions are, in most cases, highly regioselective but lead mainly to the unexpected regioisomers.",

author = "F. Zutterman and A. Krief",

year = "1983",

month = jan,

day = "1",

language = "English",

volume = "48",

pages = "1135--1137",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

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TY - JOUR

T1 - Synthesis and Diels-Alder reactions of allylidenecyclopropane [4]

AU - Zutterman, F.

AU - Krief, A.

PY - 1983/1/1

Y1 - 1983/1/1

N2 - Allylidenecyclopropane, readily available from 1-lithio-1-(phenylthio)cyclopropane, reacts with a large variety of electrophilic olefins and produces functionalized spirooctenes. The reactions are, in most cases, highly regioselective but lead mainly to the unexpected regioisomers.

AB - Allylidenecyclopropane, readily available from 1-lithio-1-(phenylthio)cyclopropane, reacts with a large variety of electrophilic olefins and produces functionalized spirooctenes. The reactions are, in most cases, highly regioselective but lead mainly to the unexpected regioisomers.

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M3 - Article

AN - SCOPUS:0002315059

VL - 48

SP - 1135

EP - 1137

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 7

ER -