1322775-64-3Relevant articles and documents
Synthesis of γ-benzopyranone by TfOH-promoted regioselective cyclization of o-alkynoylphenols
Yoshida, Masahito,Fujino, Yuta,Doi, Takayuki
, p. 4526 - 4529 (2011)
Regioselective cyclization of o-alkynoylphenols forming γ-benzopyranones has been demonstrated. Trifluoromethanesulfonic acid (TfOH) induced 6-endo cyclization of o-alkynoylphenols without forming 5-exo cyclized benzofuranone derivatives to provide the corresponding γ-benzopyranones in high yields.
Regioselective synthesis of flavone derivatives via DMAP-catalyzed cyclization of o-alkynoylphenols
Yoshida, Masahito,Fujino, Yuta,Saito, Koya,Doi, Takayuki
experimental part, p. 9993 - 9997 (2012/02/06)
A catalytic amount of DMAP promoted cyclization of o-alkynoylphenols via a 6-endo cyclization mode leading to flavone derivatives in high yields without forming 5-exo cyclized aurone derivatives. Utilizing this method, methoxy substituted flavone and alkyl substituted γ-benzopyranone derivatives were synthesized.