174967-28-3Relevant articles and documents
Indium triflate catalyzed rearrangement of aryl-substituted cyclopropyl carbinols to 1,4-disubstituted 1,3-butadienes
Ranu, Brindaban C.,Banerjee, Subhash
, p. 3012 - 3015 (2007/10/03)
Aryl-substituted cyclopropyl carbinol derivatives undergo a facile stereoselective rearrangement catalyzed by In(OTf)3 in dichloromethane under sonication to produce the substituted conjugated all-trans-butadienes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.
Catalysis by ionic liquids: Cyclopropyl carbinyl rearrangements catalyzed by [pmim]Br under organic solvent free conditions
Ranu, Brindaban C.,Banerjee, Subhash,Das, Arijit
, p. 881 - 884 (2007/10/03)
Aryl substituted cyclopropyl carbinol derivatives undergo stereoselective rearrangements catalyzed by the ionic liquid, 1-methyl-3-pentylimidazolium bromide, under sonication, without any organic solvent, to produce the substituted conjugated all-trans-butadienes.