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Changing the Reaction Pathway by NHC/Brønsted Base Cooperative Catalysis: Highly Stereoselective Synthesis of Multifunctional Benzo[a]fluoren-11-ones from the Dimerization of 2‑(Aroylvinyl)arylaldehydes

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Figshare2016-02-18 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Changing_the_Reaction_Pathway_by_NHC_Br_nsted_Base_Cooperative_Catalysis_Highly_Stereoselective_Synthesis_of_Multifunctional_Benzo_i_a_i_fluoren_11_ones_from_the_Dimerization_of_2_Aroylvinyl_arylaldehydes/2316796
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The unprecedented NHC/Brønsted base-cocatalyzed dimerization reaction of 2-(aroylvinyl)­arylaldehydes was reported. In the presence of a triazole carbene catalyst alone, no reaction of 2-(aroylvinyl)­arylaldehydes was observed. However, the combination of triazole carbene and 4-methoxyphenolate efficiently catalyzed the dimerization of 2-(aroylvinyl)­arylaldehydes to proceed through a benzoin–Michael–Michael reaction cascade, producing 6-aroyl-5-(aroylmethyl)-11a-hydroxybenzo­[a]­fluoren-11-ones as the sole diastereomers in good yields.
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2016-02-18
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