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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.