Standard

Carbonylation of chlorobiphenyls catalyzed by modified cobalt carbonyl. / Boyarskii, V. P.; Zhesko, T. E.; Tvorogov, K. E.

в: Russian Journal of Organic Chemistry, Том 43, № 12, 12.2007, стр. 1760-1764.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Boyarskii, VP, Zhesko, TE & Tvorogov, KE 2007, 'Carbonylation of chlorobiphenyls catalyzed by modified cobalt carbonyl', Russian Journal of Organic Chemistry, Том. 43, № 12, стр. 1760-1764. https://doi.org/10.1134/S1070428007120044

APA

Boyarskii, V. P., Zhesko, T. E., & Tvorogov, K. E. (2007). Carbonylation of chlorobiphenyls catalyzed by modified cobalt carbonyl. Russian Journal of Organic Chemistry, 43(12), 1760-1764. https://doi.org/10.1134/S1070428007120044

Vancouver

Boyarskii VP, Zhesko TE, Tvorogov KE. Carbonylation of chlorobiphenyls catalyzed by modified cobalt carbonyl. Russian Journal of Organic Chemistry. 2007 Дек.;43(12):1760-1764. https://doi.org/10.1134/S1070428007120044

Author

Boyarskii, V. P. ; Zhesko, T. E. ; Tvorogov, K. E. / Carbonylation of chlorobiphenyls catalyzed by modified cobalt carbonyl. в: Russian Journal of Organic Chemistry. 2007 ; Том 43, № 12. стр. 1760-1764.

BibTeX

@article{44193c3ea94646fba1b157310d939fe1,
title = "Carbonylation of chlorobiphenyls catalyzed by modified cobalt carbonyl",
abstract = "Dichlorobiphenyls having both chlorine atoms in the same benzene ring undergo mild carbonylation in the presence of 1,2-epoxypropane-modified carbonyl cobalt complex to give biphenylcarboxylic acid esters. Monochlorobiphenyls fail to react under analogous conditions. The rate and selectivity of the reaction depend on the position of chlorine atoms. Carbonylation of dichlorobiphenyls having a chlorine atom in the meta position occurs preferentially at that position. 2,4-Dichlorobiphenyl gives rise mainly to the carbonylation product at the 2-position.",
author = "Boyarskii, {V. P.} and Zhesko, {T. E.} and Tvorogov, {K. E.}",
year = "2007",
month = dec,
doi = "10.1134/S1070428007120044",
language = "English",
volume = "43",
pages = "1760--1764",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "12",

}

RIS

TY - JOUR

T1 - Carbonylation of chlorobiphenyls catalyzed by modified cobalt carbonyl

AU - Boyarskii, V. P.

AU - Zhesko, T. E.

AU - Tvorogov, K. E.

PY - 2007/12

Y1 - 2007/12

N2 - Dichlorobiphenyls having both chlorine atoms in the same benzene ring undergo mild carbonylation in the presence of 1,2-epoxypropane-modified carbonyl cobalt complex to give biphenylcarboxylic acid esters. Monochlorobiphenyls fail to react under analogous conditions. The rate and selectivity of the reaction depend on the position of chlorine atoms. Carbonylation of dichlorobiphenyls having a chlorine atom in the meta position occurs preferentially at that position. 2,4-Dichlorobiphenyl gives rise mainly to the carbonylation product at the 2-position.

AB - Dichlorobiphenyls having both chlorine atoms in the same benzene ring undergo mild carbonylation in the presence of 1,2-epoxypropane-modified carbonyl cobalt complex to give biphenylcarboxylic acid esters. Monochlorobiphenyls fail to react under analogous conditions. The rate and selectivity of the reaction depend on the position of chlorine atoms. Carbonylation of dichlorobiphenyls having a chlorine atom in the meta position occurs preferentially at that position. 2,4-Dichlorobiphenyl gives rise mainly to the carbonylation product at the 2-position.

UR - http://www.scopus.com/inward/record.url?scp=60449114444&partnerID=8YFLogxK

U2 - 10.1134/S1070428007120044

DO - 10.1134/S1070428007120044

M3 - Article

AN - SCOPUS:60449114444

VL - 43

SP - 1760

EP - 1764

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 12

ER -

ID: 87471837