Аннотация:
The review analyzes actual data on the use of polyfluorinated triarylboranes, diarylborinic and arylboronic acids as catalysts for organic reactions, e.g., hydrogenation of unsaturated bonds and alkylation of aromatic compounds.
Образец цитирования:
N. Yu. Adonin, V. V. Bardin, “Polyfluorinated arylboranes as catalysts in organic synthesis”, Mendeleev Commun., 30:3 (2020), 262–272
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1166
https://www.mathnet.ru/rus/mendc/v30/i3/p262
Эта публикация цитируется в следующих 6 статьяx:
Lars Longwitz, Reuben B. Leveson-Gower, Henriëtte J. Rozeboom, Andy-Mark W. H. Thunnissen, Gerard Roelfes, “Boron catalysis in a designer enzyme”, Nature, 629:8013 (2024), 824
Lars Longwitz, Marijn D. Kamer, Bart Brouwer, Andy-Mark W. H. Thunnissen, Gerard Roelfes, “Boron Designer Enzyme with a Hybrid Catalytic Dyad”, ACS Catal., 2024, 18469
Mikhail M. Shmakov, Sergey A. Prikhod'ko, Roman Yu Peshkov, Vadim V. Bardin, Nicolay Yu Adonin, “Aryldifluoroboranes: Lewis acidity and catalytic activity in the alkylation of phenols”, Molecular Catalysis, 521 (2022), 112202
Agnieszka Adamczyk-Woźniak, Andrzej Sporzyński, “Merging Electron Deficient Boronic Centers with Electron-Withdrawing Fluorine Substituents Results in Unique Properties of Fluorinated Phenylboronic Compounds”, Molecules, 27:11 (2022), 3427
Jian-Fei Bai, Jianbo Tang, Xiaolong Gao, Zhi-Jiang Jiang, Bencan Tang, Jia Chen, Zhanghua Gao, “Regioselective Cycloaddition and Substitution Reaction of Tertiary Propargylic Alcohols and Heteroareneboronic Acids via Acid Catalysis”, Org. Lett., 24:25 (2022), 4507
Hannah L. D. Hayes, Ran Wei, Michele Assante, Katherine J. Geogheghan, Na Jin, Simone Tomasi, Gary Noonan, Andrew G. Leach, Guy C. Lloyd-Jones, “Protodeboronation of (Hetero)Arylboronic Esters: Direct versus Prehydrolytic Pathways and Self-/Auto-Catalysis”, J. Am. Chem. Soc., 143:36 (2021), 14814
Обратная связь: