Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions
AU - Sadchikova, E. V.
AU - Mokrushin, V. S.
N1 - This work was financially supported by the Russian Foundation for Basic Research (Project No. 04 03 96121a).
PY - 2005/2/1
Y1 - 2005/2/1
N2 - The comparative reactivity of heterocyclic diazo compounds and the corresponding diazonium salts in C-azo coupling reactions was studied using imidazole, pyrazole, and triazole derivatives as examples.The reactivities of pyrazole- and imidazole-derived diazonium salts are much lower than those of thiadiazole- and 1,2,4-triazole-derived diazonium salts but higher than those of pyrrole and indole diazo compounds.
AB - The comparative reactivity of heterocyclic diazo compounds and the corresponding diazonium salts in C-azo coupling reactions was studied using imidazole, pyrazole, and triazole derivatives as examples.The reactivities of pyrazole- and imidazole-derived diazonium salts are much lower than those of thiadiazole- and 1,2,4-triazole-derived diazonium salts but higher than those of pyrrole and indole diazo compounds.
UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000231336600010
UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=25444472096
U2 - 10.1007/s11172-005-0259-7
DO - 10.1007/s11172-005-0259-7
M3 - Article
VL - 54
SP - 354
EP - 365
JO - Russian Chemical Bulletin
JF - Russian Chemical Bulletin
SN - 1066-5285
IS - 2
ER -
ID: 41351117