5765-84-4Relevant academic research and scientific papers
Synthesis and antimicrobial activities of gold(I) sulfanylcarboxylates
Barreiro, Elena,Casas, Jose S.,Couce, Maria D,Sanchez, Agustin,Seoane, Rafael,Perez-Estevez, Antonio,Sordo, Jose
body text, p. 23 - 34 (2012/07/28)
Reaction of NaAuCl4H2O and thiodiglycol (1:3 molar ratio) with 3-(aryl)-2-sulfanylpropenoic acids, H2xspa0[x:p03-phenyl- , f03-(2-furyl)-, t03-(2-thienyl)-, o-py03-(2-pyridyl)-, Clp03-(2-chlorophenyl)- , -o-mp03- (2-methox
Formation of 3-sulfanylcoumarins by SnPh3OH-promoted cyclization of 3-aryl-2-sulfanylpropenoic acids
Alvarez-Boo, Pedro,Casas, Jose S.,Couce, Maria D.,Fernandez-Moreira, Vanesa,Freijanes, Eduardo,Garcia-Martinez, Emilia,Sordo, Jose,Vazquez-Lopez, Ezequiel
, p. 4425 - 4429 (2007/10/03)
Reaction of SnPh3OH with 3-(2-hydroxyphenyl)sulfanylpropenoic acid [H2(o-hpspa)] yielded [SnPh3(SC)], where SC is deprotonated 3-sulfanylcoumarin (3-sulfanyl-2H-1-benzopyran-2-one, HSC), by a cyclization process. Similarly, when 3-(2-hydroxy-5-bromophenyl)- and 3-(2-hydroxy-3,5-dibromophenyl)-2-sulfanylpropenoic acids were treated with the same tin hydroxide, the cyclization resulted in [SnPh3(BrSC)] and [SnPh3(Br2SC)], where BrSC and Br2SC are the new ligands formed from the deprotonation of 3-sulfanyl-6-bromocoumarin and 3-sulfanyl-6,8-dibromocoumarin, respectively. The new compounds were characterized by elemental analysis, multinuclear NMR (1H, 13C and 119Sn) and vibrational spectroscopy, and mass spectrometry. Single-crystal X-ray structures of these complexes all showed that the tin atom is surrounded by three phenyl C atoms and the S and O atoms of the bidentate ligand in a distorted trigonal-bipyramidal environment. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.
