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中文摘要：
有代替的吲哚的 o-alkynylbenzaldehydes 或 o-alkynylbenzaldimines 的催化双人脚踏车反应由羰基或 imine 组的吲哚的分子间的增加开始了的 Pd (II ) 由 intramolecular 炔属羟的 nucleopalladation 列在后面，由 protonolysis 熄灭碳钯契约改革 Pd (II ) 种类被开发。没有一个氧化还原作用系统的必要性，反应能在温和条件下面被执行。
英文摘要：
A Pd（II） catalyzed tandem reaction of o-alkynylbenzaldehydes or o-alkynylbenzaldimines with substituted indoles initiated by the intermolecular addition of indoles to the carbonyl or imine group followed by the nucleopalladation of an intramolecular alkyne and quenching the carbon-palladium bond by protonolysis to regenerate the Pd（II） species was developed. The reaction can be carried out under mild conditions without the necessity of a redox system.
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