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^*

^*此作品的通信作者

研究成果: 雜誌貢獻 › 期刊論文 › 同行評審

45 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 12月 9
對外發佈	是

ASJC Scopus subject areas

催化
物理與理論化學
有機化學
無機化學

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10.1016/S0957-4166(02)00741-3

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

note = "Funding Information: We thank the National Science Council, Republic of China for the financial support.",

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AU - Wu, Hsyueh Liang

AU - Uang, Biing Jiun

N1 - Funding Information: We thank the National Science Council, Republic of China for the financial support.

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 - https://www.scopus.com/pages/publications/0037049386

UR - https://www.scopus.com/pages/publications/0037049386#tab=citedBy

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

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

M3 - Article

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SN - 0957-4166

VL - 13

SP - 2625

EP - 2628

JO - Tetrahedron Asymmetry

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IS - 24

ER -

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

摘要

ASJC Scopus subject areas

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