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

Research output: Contribution to journal › Article › peer-review

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.

Original language	English
Pages (from-to)	3545-3548
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	25
DOIs	https://doi.org/10.1016/S0040-4039(00)94438-1
Publication status	Published - 1 Jan 1990
Externally published	Yes

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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,

day = "1",

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

language = "English",

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pages = "3545--3548",

journal = "Tetrahedron Letters",

issn = "0040-4039",

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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.

Abstract

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