Facile Deboronation of Some o ‐Carboranylamides
Author:
Affiliation:
1. School of Chemistry and Chemical Engineering University of Jinan 336 West Nanxinzhuang Road 250022 Jinan P. R. China
2. Department of Chemistry New York University 100 Washington Square East 10003 New York NY USA
Funder
National Natural Science Foundation of China
Natural Science Foundation of Shandong Province
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejic.201700612
Reference23 articles.
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3. Carbaboranes as Pharmacophores: Properties, Synthesis, and Application Strategies
4. Boron in Drug Discovery: Carboranes as Unique Pharmacophores in Biologically Active Compounds
5. c)Y.‐H.Zhu N. S.Hosmane J. Organomet. Chem.2017 https://doi.org/10.1016/j.jorganchem.2017.02.020
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1. Synthesis of Bis(Carboranyl)amides 1,1′-μ-(CH2NH(O)C(CH2)n-1,2-C2B10H11)2 (n = 0, 1) and Attempt of Synthesis of Gadolinium Bis(Dicarbollide);Molecules;2021-03-02
2. Highly efficient aggregation-induced emission and stimuli-responsive fluorochromism triggered by carborane-induced charge transfer state;Inorganic Chemistry Communications;2019-08
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