Frontispiece: Direct Nucleophilic Substitution Reaction of Cage B−H Bonds by Grignard Reagents: A Route to Regioselective B4‐Alkylation of  o ‐Carboranes | Zendy

Tang Cen | Zendy; Zhang Jiji | Zendy; Xie Zuowei | Zendy

Premium

Frontispiece: Direct Nucleophilic Substitution Reaction of Cage B−H Bonds by Grignard Reagents: A Route to Regioselective B4‐Alkylation of o ‐Carboranes

Author(s) -

Tang Cen,

Zhang Jiji,

Xie Zuowei

Publication year - 2017

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.201783061

Subject(s) - regioselectivity , chemistry , nucleophilic substitution , reagent , substitution reaction , alkylation , grignard reagent , nucleophilic aromatic substitution , carborane , cage , substitution (logic) , nucleophile , stereochemistry , medicinal chemistry , organic chemistry , catalysis , mathematics , combinatorics , computer science , programming language

Carborane Functionalization In their Communication on page 8642 ff., Z. Xie and co‐workers report the first nucleophilic substitution reaction of cage B−H bonds in o ‐carboranes by Grignard reagents in the absence of any transition metals.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research