Cyclic carboxylic anhydrides as new reagents for formation of chromone ring
The propensity of cyclic carboxylic anhydrides to undergo ring-opening was exploited in a reaction with 2'-hydroxy-α-heteroarylacetophenones leading to the formation of chromones. New simple method was developed for the synthesis of 2-(ω-carboxyalkyl)-3-h
Frasinyuk, Mykhaylo S.,Bondarenko, Svitlana P.,Gorbulenko, Nataliia V.,Turov, Alexander V.,Khilya, Volodymyr P.
p. 768 - 774
(2014/06/10)
More Articles about upstream products of 1217314-90-3