Palladium-Catalyzed Asymmetric Ring-Opening Reactions of Oxabenzonorbornadienes with Potassium Trifluoroborate Salts

被引：0
|
作者：
Tao, Pingfang [1 ]
Huang, Jun [1 ,2 ]
Liu, Yuzhao [1 ]
Wei, Guangming [1 ]
Wang, Yifei [1 ]
Wei, Xiansheng [1 ]
Huang, Guobao [1 ]
Li, Xiuying [1 ]
机构：
[1] Yulin Normal Univ, Coll Chem & Food Sci, Guangxi Key Lab Agr Resources Chem & Biotechnol, Yulin 537000, Guangxi, Peoples R China
[2] Nanning Normal Univ, Coll Chem & Mat, Nanning 530001, Peoples R China
来源：
CHINESE JOURNAL OF ORGANIC CHEMISTRY | 2020年 / 40卷 / 06期
基金：
中国国家自然科学基金;
关键词：
oxabenzonorbornadiene; trifluoroborate salt; asymmetric ring-opening reaction; OXABICYCLIC ALKENES; AZABICYCLIC ALKENES; ARYLBORONIC ACIDS; BORONIC ACIDS; 2-SUBSTITUTED 1,2-DIHYDRO-1-NAPHTHOLS; BICYCLIC ALKENES; COMPLEXES; METATHESIS; REAGENTS; ROUTE;
D O I：
10.6023/cjoc201912030
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A new. versatile and highly efficient palladium-catalyzed asymmetric ring-opening reaction of oxabenzonorbomadienes with a wide range of potassium trifluoroborate salts was developed. The corresponding cis-2-aryl-1,2-dihydronaphthalen-1-ol products were obtained in good yields with moderate to good enantioselectivities under mild conditions.
引用
收藏
页码：1630 / 1637
页数：8
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