Frontispiece: Diastereoselective Synthesis of P‐Chirogenic and Atropisomeric 2,2′‐Bisphosphino‐1,1′‐binaphthyls Enabled by Internal Phosphine Oxide Directing Groups | Zendy

Xue Qingquan | Zendy; Huo Shangfei | Zendy; Wang Tingyi | Zendy; Wang Zeming | Zendy; Li Jianli | Zendy; Zhu Meifang | Zendy; Zuo Weiwei | Zendy

Premium

Frontispiece: Diastereoselective Synthesis of P‐Chirogenic and Atropisomeric 2,2′‐Bisphosphino‐1,1′‐binaphthyls Enabled by Internal Phosphine Oxide Directing Groups

Author(s) -

Xue Qingquan,

Huo Shangfei,

Wang Tingyi,

Wang Zeming,

Li Jianli,

Zhu Meifang,

Zuo Weiwei

Publication year - 2020

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Reports

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.202082162

Subject(s) - ligand (biochemistry) , phosphine , phosphine oxide , asymmetric hydrogenation , ruthenium , chemistry , catalysis , enantioselective synthesis , organic chemistry , receptor , biochemistry

Asymmetric Hydrogenation In their Research Article on page 8153, M. Zhu, W. Zuo et al. report a chiral diphosphine ligand that is both atropoisomeric and P‐chirogenic. A ruthenium–ligand catalyst exhibits good enantioselectivity in the asymmetric hydrogenation of 3‐methyl‐2‐butanone.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research