Under the proper condltions of temperature, pressure, and reagent concentration it can react violently with acetaldehyde, acetylene, acetone, secondary alcohols (e.g., 2-propanol, 2-butanol) aluminum, Al(BH4)3, AH3, aluminumtitanium alloys, alkali metals @hum, cesium, potassium, rubidlum, ...
Our reaction can be extended to the synthesis of triflavonoids by reacting2a(radical precursor) with nucleophilic flavones. These triflavones share the same type of interflavonyl bonds with the general formula of Lu-(2′-6)-Lu-(2′-6)-FL (FL = apigenin (3b), Supplementary Fig.21) diosm...
In one aspect the present invention provides a compound of formula (I):wherein: R1 and R2 are each independently selected from the group consisting of: H, halogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, heteroalkyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl, ...