Allylation of carbonyl compounds in the presence of catalytic electrogenerated zinc. Unusual regioselectivity with a trifluorinated analog of prenyl bromide

C. Gosmini; Y. Rollin; J. Perichon; C. Wakselman; M. Tordeux; L. Marival

doi:10.1016/S0040-4020(97)00280-9

Allylation of carbonyl compounds in the presence of catalytic electrogenerated zinc. Unusual regioselectivity with a trifluorinated analog of prenyl bromide

C. Gosmini
, Y. Rollin
, J. Perichon
, C. Wakselman
, M. Tordeux
, L. Marival

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

Abstract

A mild and effective method of electrochemical zinc activation based on the cathodic reduction of a catalytic amount of ZnBr₂ in acetonitrile is applied to the coupling of a trifluorinated analog of prenyl bromide with carbonyl compounds and affords unusual regioselectivity.

Original language	English
Pages (from-to)	6027-6034
Number of pages	8
Journal	Tetrahedron
Volume	53
Issue number	17
DOIs	https://doi.org/10.1016/S0040-4020(97)00280-9
Publication status	Published - 1 Jan 1997

Access to Document

10.1016/S0040-4020(97)00280-9

Cite this

@article{4fcb361b3f864d11a421f3b363a7ebd6,

title = "Allylation of carbonyl compounds in the presence of catalytic electrogenerated zinc. Unusual regioselectivity with a trifluorinated analog of prenyl bromide",

abstract = "A mild and effective method of electrochemical zinc activation based on the cathodic reduction of a catalytic amount of ZnBr2 in acetonitrile is applied to the coupling of a trifluorinated analog of prenyl bromide with carbonyl compounds and affords unusual regioselectivity.",

author = "C. Gosmini and Y. Rollin and J. Perichon and C. Wakselman and M. Tordeux and L. Marival",

year = "1997",

month = jan,

day = "1",

doi = "10.1016/S0040-4020(97)00280-9",

language = "English",

volume = "53",

pages = "6027--6034",

journal = "Tetrahedron",

issn = "0040-4020",

number = "17",

}

TY - JOUR

T1 - Allylation of carbonyl compounds in the presence of catalytic electrogenerated zinc. Unusual regioselectivity with a trifluorinated analog of prenyl bromide

AU - Gosmini, C.

AU - Rollin, Y.

AU - Perichon, J.

AU - Wakselman, C.

AU - Tordeux, M.

AU - Marival, L.

PY - 1997/1/1

Y1 - 1997/1/1

N2 - A mild and effective method of electrochemical zinc activation based on the cathodic reduction of a catalytic amount of ZnBr2 in acetonitrile is applied to the coupling of a trifluorinated analog of prenyl bromide with carbonyl compounds and affords unusual regioselectivity.

AB - A mild and effective method of electrochemical zinc activation based on the cathodic reduction of a catalytic amount of ZnBr2 in acetonitrile is applied to the coupling of a trifluorinated analog of prenyl bromide with carbonyl compounds and affords unusual regioselectivity.

U2 - 10.1016/S0040-4020(97)00280-9

DO - 10.1016/S0040-4020(97)00280-9

M3 - Article

AN - SCOPUS:0030900981

SN - 0040-4020

VL - 53

SP - 6027

EP - 6034

JO - Tetrahedron

JF - Tetrahedron

IS - 17

ER -

Allylation of carbonyl compounds in the presence of catalytic electrogenerated zinc. Unusual regioselectivity with a trifluorinated analog of prenyl bromide

Abstract

Access to Document

Fingerprint

Cite this