26106-48-9Relevant academic research and scientific papers
Synthesis of β,β-Dichlorosulfides and Their Reactions with Thiols
Arkhipov,Romanova,Anisimov
, p. 530 - 533 (2007/10/03)
Reaction of allyl aryl ethers with sulfur dichloride at of reagents ratio 2:1 proceeds regioselectively with the formation of β,β-dichlorosulfides as the products of Markovnikoff and anti-Markovnikoff addition to the double bond of the allyl group, wherea
Molecule Linkage by Sulfur Chlorides. VIII. The Rearrangement of the Anti-Markovnikov 2:1-Adducts from Allyl-phenyl-ethers and Sulfur Dichloride to the Regioisomeric Compounds
Hollmann, K.,Moeder, M.,Muehlstaedt, M.,Kleinpeter, E.,Habermann, B.
, p. 503 - 508 (2007/10/02)
The anti-Markovnikov 2:1-adducts 2 (bis-(1-chlor-3-phenoxy-prop-2-yl)-sulfane) of allyl-phenyl-ethers 1 have been rearranged by refluxing in ethanol to the regioisomers 3 (bis-(2-chlor-3-phenoxy-prop-1-yl)-sulfane).The products were identified by 1H-n.m.r
