Oxidation of allylselenides with the sharpless AD-reagents

A. Krief; C. Colaux; W. Dumont

doi:10.1016/S0040-4039(97)00596-0

Oxidation of allylselenides with the sharpless AD-reagents

A. Krief, C. Colaux, W. Dumont

Unite de recherche en chimie organique

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

Résumé

Allylselenides are efficiently oxidized by AD-mix reagents. Oxidation takes chemoselectively place on the selenium atom of allylselenides bearing a methylseleno or a phenylseleno moiety, but chemoselectively occurs on the C,C double bond of the corresponding o-nitrophenyl derivatives.

langue originale	Anglais
Pages (de - à)	3315-3318
Nombre de pages	4
journal	Tetrahedron Letters
Volume	38
Numéro de publication	18
Les DOIs	https://doi.org/10.1016/S0040-4039(97)00596-0
Etat de la publication	Publié - 5 mai 1997

Accès au document

10.1016/S0040-4039(97)00596-0

Autres fichiers et liens

Link to publication in Scopus

Contient cette citation

@article{90a0d9b1851b4607a9d7150b1e22b46f,

title = "Oxidation of allylselenides with the sharpless AD-reagents",

abstract = "Allylselenides are efficiently oxidized by AD-mix reagents. Oxidation takes chemoselectively place on the selenium atom of allylselenides bearing a methylseleno or a phenylseleno moiety, but chemoselectively occurs on the C,C double bond of the corresponding o-nitrophenyl derivatives.",

author = "A. Krief and C. Colaux and W. Dumont",

year = "1997",

month = may,

day = "5",

doi = "10.1016/S0040-4039(97)00596-0",

language = "English",

volume = "38",

pages = "3315--3318",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "18",

}

TY - JOUR

T1 - Oxidation of allylselenides with the sharpless AD-reagents

AU - Krief, A.

AU - Colaux, C.

AU - Dumont, W.

PY - 1997/5/5

Y1 - 1997/5/5

N2 - Allylselenides are efficiently oxidized by AD-mix reagents. Oxidation takes chemoselectively place on the selenium atom of allylselenides bearing a methylseleno or a phenylseleno moiety, but chemoselectively occurs on the C,C double bond of the corresponding o-nitrophenyl derivatives.

AB - Allylselenides are efficiently oxidized by AD-mix reagents. Oxidation takes chemoselectively place on the selenium atom of allylselenides bearing a methylseleno or a phenylseleno moiety, but chemoselectively occurs on the C,C double bond of the corresponding o-nitrophenyl derivatives.

UR - http://www.scopus.com/inward/record.url?scp=0030938842&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(97)00596-0

DO - 10.1016/S0040-4039(97)00596-0

M3 - Article

AN - SCOPUS:0030938842

SN - 0040-4039

VL - 38

SP - 3315

EP - 3318

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 18

ER -

Oxidation of allylselenides with the sharpless AD-reagents

Résumé

Accès au document

Autres fichiers et liens

Empreinte digitale

Contient cette citation