Asymmetric epoxidation of allylic alcohols catalyzed by new chiral vanadium(V) complexes

Hsyueh-Liang Wu; Biing Jiun Uang

doi:10.1016/S0957-4166(02)00741-3

Asymmetric epoxidation of allylic alcohols catalyzed by new chiral vanadium(V) complexes

Hsyueh-Liang Wu, Biing Jiun Uang

化學系

研究成果: 雜誌貢獻 › 文章 › 同行評審

39 引文斯高帕斯（Scopus）

摘要

Vanadium catalysts bearing (+)-ketopinic acid-based chiral hydroxamic acids as constituent ligands are investigated in the asymmetric epoxidation of allylic alcohols. Chiral ligands lacking an N-substituent and those having a bulkier aryl group in the bornane skeleton provided better selectivity.

原文	英語
頁（從 - 到）	2625-2628
頁數	4
期刊	Tetrahedron Asymmetry
卷	13
發行號	24
DOIs	https://doi.org/10.1016/S0957-4166(02)00741-3
出版狀態	已發佈 - 2002 十二月 9

ASJC Scopus subject areas

Catalysis
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

存取文件

10.1016/S0957-4166(02)00741-3

指紋深入研究「Asymmetric epoxidation of allylic alcohols catalyzed by new chiral vanadium(V) complexes」主題。共同形成了獨特的指紋。

引用此

@article{50f928d21d744882b8f99b8581cdc9b0,

title = "Asymmetric epoxidation of allylic alcohols catalyzed by new chiral vanadium(V) complexes",

abstract = "Vanadium catalysts bearing (+)-ketopinic acid-based chiral hydroxamic acids as constituent ligands are investigated in the asymmetric epoxidation of allylic alcohols. Chiral ligands lacking an N-substituent and those having a bulkier aryl group in the bornane skeleton provided better selectivity.",

author = "Hsyueh-Liang Wu and Uang, {Biing Jiun}",

year = "2002",

month = dec,

day = "9",

doi = "10.1016/S0957-4166(02)00741-3",

language = "English",

volume = "13",

pages = "2625--2628",

journal = "Tetrahedron Asymmetry",

issn = "0957-4166",

publisher = "Elsevier Limited",

number = "24",

}

TY - JOUR

T1 - Asymmetric epoxidation of allylic alcohols catalyzed by new chiral vanadium(V) complexes

AU - Wu, Hsyueh-Liang

AU - Uang, Biing Jiun

PY - 2002/12/9

Y1 - 2002/12/9

N2 - Vanadium catalysts bearing (+)-ketopinic acid-based chiral hydroxamic acids as constituent ligands are investigated in the asymmetric epoxidation of allylic alcohols. Chiral ligands lacking an N-substituent and those having a bulkier aryl group in the bornane skeleton provided better selectivity.

AB - Vanadium catalysts bearing (+)-ketopinic acid-based chiral hydroxamic acids as constituent ligands are investigated in the asymmetric epoxidation of allylic alcohols. Chiral ligands lacking an N-substituent and those having a bulkier aryl group in the bornane skeleton provided better selectivity.

UR - http://www.scopus.com/inward/record.url?scp=0037049386&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0037049386&partnerID=8YFLogxK

U2 - 10.1016/S0957-4166(02)00741-3

DO - 10.1016/S0957-4166(02)00741-3

M3 - Article

AN - SCOPUS:0037049386

VL - 13

SP - 2625

EP - 2628

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

SN - 0957-4166

IS - 24

ER -