Multiple radical additions starting with iminyl radicals derived from sulphenylimines.

Jean Boivin; Eric Fouquet; Samir Z. Zard

doi:10.1016/S0040-4039(00)94438-1

Multiple radical additions starting with iminyl radicals derived from sulphenylimines.

Jean Boivin
, Eric Fouquet
, Samir Z. Zard

Laboratoire de Synthèse Organique

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

34 Citations (Scopus)

Résumé

Iminyl radicals obtained by tri-n-butylstannane induced cleavage of S-phenyl sulphenylimines readily cyclise onto suitably located double bonds. The intermediate carbon centered radical can be trapped by a variety of electron-poor olefins thus providing an entry into synthetically useful pyrroline derivatives.

langue originale	Anglais
Pages (de - à)	3545-3548
Nombre de pages	4
journal	Tetrahedron Letters
Volume	31
Numéro de publication	25
Les DOIs	https://doi.org/10.1016/S0040-4039(00)94438-1
état	Publié - 1 janv. 1990
Modification externe	Oui

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10.1016/S0040-4039(00)94438-1

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@article{6447052040054a01bfd0b069acb6acb3,

title = "Multiple radical additions starting with iminyl radicals derived from sulphenylimines.",

abstract = "Iminyl radicals obtained by tri-n-butylstannane induced cleavage of S-phenyl sulphenylimines readily cyclise onto suitably located double bonds. The intermediate carbon centered radical can be trapped by a variety of electron-poor olefins thus providing an entry into synthetically useful pyrroline derivatives.",

author = "Jean Boivin and Eric Fouquet and Zard, \{Samir Z.\}",

year = "1990",

month = jan,

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doi = "10.1016/S0040-4039(00)94438-1",

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pages = "3545--3548",

journal = "Tetrahedron Letters",

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TY - JOUR

T1 - Multiple radical additions starting with iminyl radicals derived from sulphenylimines.

AU - Boivin, Jean

AU - Fouquet, Eric

AU - Zard, Samir Z.

PY - 1990/1/1

Y1 - 1990/1/1

N2 - Iminyl radicals obtained by tri-n-butylstannane induced cleavage of S-phenyl sulphenylimines readily cyclise onto suitably located double bonds. The intermediate carbon centered radical can be trapped by a variety of electron-poor olefins thus providing an entry into synthetically useful pyrroline derivatives.

AB - Iminyl radicals obtained by tri-n-butylstannane induced cleavage of S-phenyl sulphenylimines readily cyclise onto suitably located double bonds. The intermediate carbon centered radical can be trapped by a variety of electron-poor olefins thus providing an entry into synthetically useful pyrroline derivatives.

U2 - 10.1016/S0040-4039(00)94438-1

DO - 10.1016/S0040-4039(00)94438-1

M3 - Article

AN - SCOPUS:0025345704

SN - 0040-4039

VL - 31

SP - 3545

EP - 3548

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 25

ER -

Multiple radical additions starting with iminyl radicals derived from sulphenylimines.

Résumé

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