35875-01-5Relevant articles and documents
One-pot synthesis of keto thioethers by palladium/gold-catalyzed click and pinacol reactions
Cadu, Alban,Watile, Rahul A.,Biswas, Srijit,Orthaber, Andreas,Sj?berg, Per J. R.,Samec, Joseph S. M.
, p. 5556 - 5559 (2014)
An atom-efficient synthesis of keto thioethers was devised via tandem gold/palladium catalysis. The reaction proceeds through a regioselective thiol attack at the β-position of the alcohol, followed by an alkyl, aryl, or benzyl 1,2-shift. Both acyclic and cyclic systems were studied, in the latter case leading to the ring expansion of cyclic substrates.
REARRANGEMENT OF CYCLIC ALCOHOLS WITH AN ADJACENT PHENYLTHIO (PhS-) GROUP: MIGRATION OF A PhS GROUP AROUND A RING.
Hannaby, Malcolm,Warren, Stuart
, p. 765 - 768 (2007/10/02)
PhS migratoin around rings (size 5-15) gives allyl sulphides with a regioselectivity wich varies with ring size.