Publication | Closed Access
Synthesis of Rigid Analogues of Flavone by Intramolecular Heck Reaction
13
Citations
28
References
2015
Year
Diversity Oriented SynthesisDerivativesEngineeringWide Substrate ScopeDiversity-oriented SynthesisOrganic ChemistryIntramolecular Heck ReactionPharmacologySynthetic ChemistryBiomolecular EngineeringRigid AnaloguesNatural Product Synthesis
Abstract A novel concise method to synthesize rigid analogues of flavone by an intramolecular Heck reaction with wide substrate scope was developed. The key intermediates 3‐(2‐bromobenzyl)‐4 H ‐chromen‐4‐ones were prepared easily in two steps. Most compounds were obtained with moderate to good yields (34–90 % yield, 19 examples).
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