Synthetic strategies to chiral organosulfur donors related to bis (ethylenedithio) tetrathiafulvalene
JP Griffiths, H Nie, RJ Brown, P Day… - Organic & Biomolecular …, 2005 - pubs.rsc.org
Syntheses of enantiopure organosulfur donors by three different strategies requiring only
four–six steps are reported. The key step involves either double substitution of an …
four–six steps are reported. The key step involves either double substitution of an …
The role of functional nitro and cyano groups in the self‐assembly of 1, 3‐dithiole‐2‐thione–halogen adducts
PJ Skabara, A Kanibolotsky, S Render… - … Journal of Main …, 2007 - Wiley Online Library
The synthesis of five new dihalogen/interhalogen charge transfer adducts featuring cyano
and nitro functionalized 1, 3‐dithiole‐2‐thiones have been prepared and characterized by x …
and nitro functionalized 1, 3‐dithiole‐2‐thiones have been prepared and characterized by x …
6, 6-Diphenyl-6, 7-dihydro-5H-1, 3, 4, 8-tetrathia-6-stannazulene-2-thione and 6, 6′-spirobi [6, 7-dihydro-5H-1, 3, 4, 8-tetrathia-6-stannazulene]-2, 2′-dithione
WTA Harrison, RA Howie, JMS Skakle… - … Section C: Crystal …, 2002 - journals.iucr.org
The title compounds,[Sn (C6H5) 2 (C5H4S5)] and [Sn (C5H4S5) 2], respectively, are of
interest because they can be regarded as intermediate in nature between chelates and …
interest because they can be regarded as intermediate in nature between chelates and …