机译:<![cdata [无金属氧化钴催化的c(sp 2℃>) - H羰基化的 ortho rOtho-rali丙氨酸:自由的方法( nh < / i>) - phenanthridinones]]>
Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education College of Pharmaceutical Sciences Zhejiang University of Technology Hangzhou 310014 People’s Republic of China;
Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education College of Pharmaceutical Sciences Zhejiang University of Technology Hangzhou 310014 People’s Republic of China;
Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education College of Pharmaceutical Sciences Zhejiang University of Technology Hangzhou 310014 People’s Republic of China;
Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education College of Pharmaceutical Sciences Zhejiang University of Technology Hangzhou 310014 People’s Republic of China;
Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education College of Pharmaceutical Sciences Zhejiang University of Technology Hangzhou 310014 People’s Republic of China;
机译:<![cdata [无金属氧化钴催化的c(sp 2℃>) - H羰基化的 ortho rOtho-rali丙氨酸:自由的方法( nh < / i>) - phenanthridinones]]>
机译:通过无配体的铜催化环化反应有效合成(NH)-菲啶酮
机译:活化C-sp2-H和C-sp3-H键的羰基化方法:铜催化的咪唑并[1,2-a]吡啶与甲基戊烯的区域选择性交叉偶联
机译:氨基喹啉指导钴催化的磺酰胺sp2 C–H键的羰基化
机译:通过金属催化剂的无氧C(SP2)-C(SP3)吡啶(SP3)1-氨基-2-咪喹 - 吡啶和1-芳基-5-吡唑酮之间的可持续合成方法(吡唑-4- ylidene)吡啶(SP3)偶联反应