497825-38-4Relevant academic research and scientific papers
An anion receptor that facilitates transmembrane proton-anion symport by deprotonating its sulfonamide N-H proton
Shinde, Sopan Valiba,Talukdar, Pinaki
, p. 10351 - 10354 (2018)
Indole-based amide-sulfonamide derivatives were synthesized. The X-ray crystal structure and chloride binding studies in solution showed a 1?:?1 stoichiometry. The ion transport efficiency directly correlated to the pKa of the sulfonamide N-H p
N-monoacylated derivatives of o-phenylenediamines, their analogs and their use as pharmaceutical agents
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, (2008/06/13)
New compounds represented by the formula or pharmaceutically acceptable salts or prodrugs thereof, wherein X1 and X2 are each independently selected from a CH group or a nitrogen atom; and R is an optionally substituted five or six membered nonaromatic carbocyclic ring or a nonaromatic or aromatic heterocyclic ring, whereby the ring is optionally condensed with a 6-membered, optionally substituted carbocyclic aromatic ring.
SYNTHESIS OF 1H-INDOLYL-2-BENZIMIDAZOLES AND 1H-INDOLYL-2-BENZOTHIAZOLES
Hudkins, Robert L.
, p. 1045 - 1050 (2007/10/02)
A convenient synthesis of regioisomeric 1H-indolyl-2-benzimidazoles and -2-benzothiazoles by the direct conversion of indoleesters with the in situ generated organoaluminum reagents trimethylaluminum-1,2-diaminobenzene or trimethylaluminum-2-aminothiophenol is reported.
