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@article{41bf84bc36384e55868ddc3ec2a5daf5,
title = "Base-mediated intramolecular aryl–aryl coupling in pyrazolyl-containing iodolium salts",
abstract = "Pyrazolyl-containing aryliodolium salts undergo transformation to iodopyrazoles accompanied by the formation of a new Csp2-Csp2 bond in the presence of a base (DIPEA, NaOH, or K2CO3). The plausible mechanism of the base-mediated reaction is suggested. The catalytic activity of the iodine-containing species is studied in the model reaction.",
author = "Сафинская, {Яна Валерьевна} and Ильин, {Михаил Вячеславович} and Болотин, {Дмитрий Сергеевич}",
year = "2024",
month = nov,
day = "4",
doi = "10.1039/d4nj02894e",
language = "English",
journal = "New Journal of Chemistry",
issn = "1144-0546",
publisher = "Royal Society of Chemistry",

}

RIS

TY - JOUR

T1 - Base-mediated intramolecular aryl–aryl coupling in pyrazolyl-containing iodolium salts

AU - Сафинская, Яна Валерьевна

AU - Ильин, Михаил Вячеславович

AU - Болотин, Дмитрий Сергеевич

PY - 2024/11/4

Y1 - 2024/11/4

N2 - Pyrazolyl-containing aryliodolium salts undergo transformation to iodopyrazoles accompanied by the formation of a new Csp2-Csp2 bond in the presence of a base (DIPEA, NaOH, or K2CO3). The plausible mechanism of the base-mediated reaction is suggested. The catalytic activity of the iodine-containing species is studied in the model reaction.

AB - Pyrazolyl-containing aryliodolium salts undergo transformation to iodopyrazoles accompanied by the formation of a new Csp2-Csp2 bond in the presence of a base (DIPEA, NaOH, or K2CO3). The plausible mechanism of the base-mediated reaction is suggested. The catalytic activity of the iodine-containing species is studied in the model reaction.

UR - https://www.mendeley.com/catalogue/ea5275f0-d241-3538-8335-1f961aa7dc8e/

U2 - 10.1039/d4nj02894e

DO - 10.1039/d4nj02894e

M3 - Article

JO - New Journal of Chemistry

JF - New Journal of Chemistry

SN - 1144-0546

ER -

ID: 126741429