New chiral (salen)manganese(III) systems for asymmetric epoxidation of styrene

Saili Wei; Yuhai Tang; Guojin Xu; Xiaoshuang Tang; Yongjin Ling; Rui Li; Yang Sun

doi:10.1007/s11144-009-0035-z

New chiral (salen)manganese(III) systems for asymmetric epoxidation of styrene

Saili Wei
, Yuhai Tang
, Guojin Xu
, Xiaoshuang Tang
, Yongjin Ling
, Rui Li
, Yang Sun

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

8 Scopus citations

Abstract

Highly enantioselelctive and repeatable epoxidation of styrene was performed by using new chiral (salen)Mn(III) catalysts, which were derived from the initial immobilization of a homogeneous (salen)Mn(III) complex on solid carriers and subsequent dispersion into ionic liquids.

Original language	English
Pages (from-to)	329-333
Number of pages	5
Journal	Reaction Kinetics and Catalysis Letters
Volume	97
Issue number	2
DOIs	https://doi.org/10.1007/s11144-009-0035-z
State	Published - Aug 2009
Externally published	Yes

Keywords

(salen)Mn(III)
Enantioselective
Epoxidation
Ionic liquid

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10.1007/s11144-009-0035-z

Cite this

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title = "New chiral (salen)manganese(III) systems for asymmetric epoxidation of styrene",

abstract = "Highly enantioselelctive and repeatable epoxidation of styrene was performed by using new chiral (salen)Mn(III) catalysts, which were derived from the initial immobilization of a homogeneous (salen)Mn(III) complex on solid carriers and subsequent dispersion into ionic liquids.",

keywords = "(salen)Mn(III), Enantioselective, Epoxidation, Ionic liquid",

author = "Saili Wei and Yuhai Tang and Guojin Xu and Xiaoshuang Tang and Yongjin Ling and Rui Li and Yang Sun",

year = "2009",

month = aug,

doi = "10.1007/s11144-009-0035-z",

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journal = "Reaction Kinetics and Catalysis Letters",

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T1 - New chiral (salen)manganese(III) systems for asymmetric epoxidation of styrene

AU - Wei, Saili

AU - Tang, Yuhai

AU - Xu, Guojin

AU - Tang, Xiaoshuang

AU - Ling, Yongjin

AU - Li, Rui

AU - Sun, Yang

PY - 2009/8

Y1 - 2009/8

N2 - Highly enantioselelctive and repeatable epoxidation of styrene was performed by using new chiral (salen)Mn(III) catalysts, which were derived from the initial immobilization of a homogeneous (salen)Mn(III) complex on solid carriers and subsequent dispersion into ionic liquids.

AB - Highly enantioselelctive and repeatable epoxidation of styrene was performed by using new chiral (salen)Mn(III) catalysts, which were derived from the initial immobilization of a homogeneous (salen)Mn(III) complex on solid carriers and subsequent dispersion into ionic liquids.

KW - (salen)Mn(III)

KW - Enantioselective

KW - Epoxidation

KW - Ionic liquid

UR - https://www.scopus.com/pages/publications/68249111227

U2 - 10.1007/s11144-009-0035-z

DO - 10.1007/s11144-009-0035-z

M3 - 文章

AN - SCOPUS:68249111227

SN - 0133-1736

VL - 97

SP - 329

EP - 333

JO - Reaction Kinetics and Catalysis Letters

JF - Reaction Kinetics and Catalysis Letters

IS - 2

ER -

New chiral (salen)manganese(III) systems for asymmetric epoxidation of styrene

Abstract

Keywords

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