5654-93-3Relevant articles and documents
Excited-state proton phototransfer in the (3-methyl-7-azaindole)-(7- azaindole) heterodimer
Catalán, Javier,Díaz, Cristina,De Paz, José L.G.
, p. 164 - 167 (2006)
A molecule of 7-azaindole and another of 3-methyl-7-azaindole form a doubly hydrogen bonded heterodimer of Cs symmetry with a first electronic excited state a′ where the electronic excitation is highly localized on one of the molecular halves. Also, because the electronic excitation only increases the acidity of the pyrrole nucleus and the basicity of the pyridine nucleus in one of the two hydrogen bonds, the heterodimer undergoes single rather than double proton transfer.
Iridium-catalyzed methylation of indoles and pyrroles using methanol as feedstock
Chen, Shu-Jie,Lu, Guo-Ping,Cai, Chun
, p. 70329 - 70332 (2015/09/07)
Iridium-catalyzed methylation of indoles and pyrroles using methanol as the methylating agent was achieved. This transformation takes place via a borrowing hydrogen methodology under an air atmosphere, which constitutes a direct route to 3-methyl-indoles and methyl-pyrroles.
4-(BENZOIMIDAZOL-2-YL)-THIAZOLE COMPOUNDS AND RELATED AZA DERIVATIVES
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Page/Page column 92; 93, (2013/08/15)
The invention relates to compounds of Formula (I) wherein ring A, X, (R1)n, R2, R3, R4, R4', R5, n, and p are as described in the description; to pharmaceutically acceptable salts thereof, and to the use of such compounds as medicaments, especially as modulators of the CXCR3 receptor.