机译:镍催化的分子内亲核亲核加入芳基或氯乙烯至α-酮酰胺通过C-Cl键活化
State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology Zhejiang University of Technology Chaowang Road 18 Hangzhou 310014 China;
State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology Zhejiang University of Technology Chaowang Road 18 Hangzhou 310014 China;
Department of Chemistry Zhejiang Sci-Tech University Xiasha Higher Education Zone 5 Second Avenue Hangzhou 310018 China;
State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology Zhejiang University of Technology Chaowang Road 18 Hangzhou 310014 China;
State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology Zhejiang University of Technology Chaowang Road 18 Hangzhou 310014 China;
State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology Zhejiang University of Technology Chaowang Road 18 Hangzhou 310014 China;
aryl chloride; homogenous catalysis; ketoamide; nickel; nucleophilic addition;
机译:镍催化的分子内亲核亲核加入芳基或氯乙烯至α-酮酰胺通过C-Cl键活化
机译:钯催化的α-酮酰胺基芳基卤化物的分子内亲核加成反应合成3-羟基羟吲哚
机译:脂肪族乙烯基C-Cl键的活化合成二有机钴盐酸盐及其表征
机译:通过镍催化的C-N和C-O键合成杂环化合物至炔烃
机译:过渡金属催化的芳基和乙烯基叠氮化物的分子内氮原子转移反应
机译:同位素比率质谱法对氯同位素的影响表明三氯乙烯(TCE)还原脱卤中的分子内C-Cl键竞争
机译:Rücktitelbild:通过钴催化的C-H催化和分子内亲核加成(Angew.13 / 2016),对芳香/乙烯基酰胺的芳香/乙烯基酰胺的芳香/乙烯基酰胺的环化(Angew.13/2016)
机译:对活化双键的亲核加成:从电荷密度的拉普拉斯算子预测反应性