136054-86-9Relevant articles and documents
Oxidative cyclization of o-hydroxy-ω-cinnamylideneacetophenones to 2-styrylchromones with potassium iodate-dimethyl sulphoxide
Singhi, Manasi,Grover, S. K.
, p. 1083 - 1084 (2007/10/02)
o-Hydroxy-ω-cinnamylideneacetophenones (1) have been found to undergo oxidative cyclization to the corresponding 2-styrylchromones (2) in satisfactory yields by heating them with potassium iodate in dimethyl sulphoxide.
A modified synthesis of 2-styrylchromones
Makrandi, J. K.,Seema
, p. 788 - 789 (2007/10/02)
2-Hydroxy-ω-cinnamylideneacetophenones (3a-e) have been obtained by condensation of 2-hydroxyacetophenones (1) with cinnamaldehyde (2) in the presence of barium hydroxide.Oxidative cyclisation of the compounds 3a-e with iodine in dimethyl sulphoxide provi