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New approach to the generation of aryldifluoroboranes–prospective acid catalysts of organic reactions. / Shmakov, Mikhail M.; Prikhod'ko, Sergey A.; Bardin, Vadim V. et al.

In: Mendeleev Communications, Vol. 28, No. 4, 01.07.2018, p. 369-371.

Research output: Contribution to journal › Article › peer-review

Harvard

Shmakov, MM, Prikhod'ko, SA, Bardin, VV & Adonin, NY 2018, 'New approach to the generation of aryldifluoroboranes–prospective acid catalysts of organic reactions', Mendeleev Communications, vol. 28, no. 4, pp. 369-371. https://doi.org/10.1016/j.mencom.2018.07.009

APA

Shmakov, M. M., Prikhod'ko, S. A., Bardin, V. V., & Adonin, N. Y. (2018). New approach to the generation of aryldifluoroboranes–prospective acid catalysts of organic reactions. Mendeleev Communications, 28(4), 369-371. https://doi.org/10.1016/j.mencom.2018.07.009

Vancouver

Shmakov MM, Prikhod'ko SA, Bardin VV, Adonin NY. New approach to the generation of aryldifluoroboranes–prospective acid catalysts of organic reactions. Mendeleev Communications. 2018 Jul 1;28(4):369-371. doi: 10.1016/j.mencom.2018.07.009

Author

Shmakov, Mikhail M. ; Prikhod'ko, Sergey A. ; Bardin, Vadim V. et al. / New approach to the generation of aryldifluoroboranes–prospective acid catalysts of organic reactions. In: Mendeleev Communications. 2018 ; Vol. 28, No. 4. pp. 369-371.

BibTeX

@article{954176af52db40dea14281725ae272e6,
title = "New approach to the generation of aryldifluoroboranes–prospective acid catalysts of organic reactions",
abstract = "A new approach for preparation of aromatic and fluoroaromatic difluoroboranes via the interaction between corresponding aryltrifluoroborates and ionic liquids containing tetrachloroaluminate-anion and aluminum chloride has been developed. Catalytic properties of obtained aryldifluoroboranes have been investigated in model reactions of phenols alkylation. The dependence of catalytic properties on both the nature of solvent used and the type of substituents in the aromatic ring of difluoroborane has been established.[Figure presented]",
keywords = "POLYFLUOROARYL ORGANOMETALLIC COMPOUNDS",
author = "Shmakov, {Mikhail M.} and Prikhod'ko, {Sergey A.} and Bardin, {Vadim V.} and Adonin, {Nicolay Yu}",
note = "Publisher Copyright: {\textcopyright} 2018",
year = "2018",
month = jul,
day = "1",
doi = "10.1016/j.mencom.2018.07.009",
language = "English",
volume = "28",
pages = "369--371",
journal = "Mendeleev Communications",
issn = "0959-9436",
publisher = "Elsevier",
number = "4",

}

RIS

TY - JOUR

T1 - New approach to the generation of aryldifluoroboranes–prospective acid catalysts of organic reactions

AU - Shmakov, Mikhail M.

AU - Prikhod'ko, Sergey A.

AU - Bardin, Vadim V.

AU - Adonin, Nicolay Yu

N1 - Publisher Copyright: © 2018

PY - 2018/7/1

Y1 - 2018/7/1

N2 - A new approach for preparation of aromatic and fluoroaromatic difluoroboranes via the interaction between corresponding aryltrifluoroborates and ionic liquids containing tetrachloroaluminate-anion and aluminum chloride has been developed. Catalytic properties of obtained aryldifluoroboranes have been investigated in model reactions of phenols alkylation. The dependence of catalytic properties on both the nature of solvent used and the type of substituents in the aromatic ring of difluoroborane has been established.[Figure presented]

AB - A new approach for preparation of aromatic and fluoroaromatic difluoroboranes via the interaction between corresponding aryltrifluoroborates and ionic liquids containing tetrachloroaluminate-anion and aluminum chloride has been developed. Catalytic properties of obtained aryldifluoroboranes have been investigated in model reactions of phenols alkylation. The dependence of catalytic properties on both the nature of solvent used and the type of substituents in the aromatic ring of difluoroborane has been established.[Figure presented]

KW - POLYFLUOROARYL ORGANOMETALLIC COMPOUNDS

UR - http://www.scopus.com/inward/record.url?scp=85051020946&partnerID=8YFLogxK

U2 - 10.1016/j.mencom.2018.07.009

DO - 10.1016/j.mencom.2018.07.009

M3 - Article

AN - SCOPUS:85051020946

VL - 28

SP - 369

EP - 371

JO - Mendeleev Communications

JF - Mendeleev Communications

SN - 0959-9436

IS - 4

ER -

ID: 16074468