Regioselective epoxidations of dienes with manganese(III) porphyrin catalysts

Kenneth S. Suslick; Bruce R. Cook

doi:10.1039/C39870000200

Regioselective epoxidations of dienes with manganese(III) porphyrin catalysts

Kenneth S. Suslick, Bruce R. Cook

Chemistry

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

Abstract

A series of sterically hindered manganese porphyrins are shown to be shape-selective catalysts for the epoxidation of a variety of dienes; product ration differences for conjugated vs. non-conjugated dienes indicate the existence of at least two competing epoxidation pathways.

Original language	English (US)
Pages (from-to)	200-202
Number of pages	3
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	3
DOIs	https://doi.org/10.1039/C39870000200
State	Published - 1987

ASJC Scopus subject areas

Molecular Medicine

Online availability

10.1039/C39870000200

Library availability

Discover UIUC Full Text

Cite this

@article{85296f1eb6d74c3ab5ee99f8be1030ac,

title = "Regioselective epoxidations of dienes with manganese(III) porphyrin catalysts",

abstract = "A series of sterically hindered manganese porphyrins are shown to be shape-selective catalysts for the epoxidation of a variety of dienes; product ration differences for conjugated vs. non-conjugated dienes indicate the existence of at least two competing epoxidation pathways.",

author = "Suslick, {Kenneth S.} and Cook, {Bruce R.}",

year = "1987",

doi = "10.1039/C39870000200",

language = "English (US)",

pages = "200--202",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "3",

}

TY - JOUR

T1 - Regioselective epoxidations of dienes with manganese(III) porphyrin catalysts

AU - Suslick, Kenneth S.

AU - Cook, Bruce R.

PY - 1987

Y1 - 1987

N2 - A series of sterically hindered manganese porphyrins are shown to be shape-selective catalysts for the epoxidation of a variety of dienes; product ration differences for conjugated vs. non-conjugated dienes indicate the existence of at least two competing epoxidation pathways.

AB - A series of sterically hindered manganese porphyrins are shown to be shape-selective catalysts for the epoxidation of a variety of dienes; product ration differences for conjugated vs. non-conjugated dienes indicate the existence of at least two competing epoxidation pathways.

UR - http://www.scopus.com/inward/record.url?scp=37049084675&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=37049084675&partnerID=8YFLogxK

U2 - 10.1039/C39870000200

DO - 10.1039/C39870000200

M3 - Article

AN - SCOPUS:37049084675

SP - 200

EP - 202

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 3

ER -

Regioselective epoxidations of dienes with manganese(III) porphyrin catalysts

Abstract

ASJC Scopus subject areas

Online availability

Library availability

Related links

Fingerprint

Cite this