WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan.
J Am Chem Soc. 2013 Jul 17;135(28):10222-5. doi: 10.1021/ja403382d. Epub 2013 Jul 2.
A novel and selective Pd-catalyzed cascade crossover-annulation of o-alkynylarylhalides and diarylacetylenes for the synthesis of dibenzo[a,e]pentalenes has been reported. Various arylacetylenes with a wide range of functional groups were tolerated, producing the corresponding multisubstituted dibenzopentalenes with the different substituents on the aromatic rings in good to high yields under the optimized reaction conditions. The reaction proceeds through a Pd-catalyzed cascade carbopalladation and C-H activation. The use of the combined DBU and CsOPiv bases is crucial for the successful implementation of the present cross-annulation.
一种新型的 Pd 催化的 o-卤代芳基炔烃和二芳基乙炔的串联交叉环化-环化反应,用于合成二苯并[a,e]戊二烯,已经被报道。各种带有广泛官能团的芳基乙炔都可以容忍,在优化的反应条件下,以良好到高的收率得到了不同取代基的多取代二苯并戊二烯。反应经过 Pd 催化的串联碳钯化和 C-H 活化。联合使用 DBU 和 CsOPiv 碱对于本交叉环化的成功实施至关重要。