机译:前封面图片:无痕指示组辅助钴催化的C?H苄胺的C?H羰基化(ADC。合成。催讯。2017年2月21日)
Key Laboratory of Pharmaceutical Engineering of Ministry of Education College of Pharmaceutical ScienceZhejiang University of TechnologyHangzhou 310014 People's Republic of China;
Key Laboratory of Pharmaceutical Engineering of Ministry of Education College of Pharmaceutical ScienceZhejiang University of TechnologyHangzhou 310014 People's Republic of China;
Key Laboratory of Pharmaceutical Engineering of Ministry of Education College of Pharmaceutical ScienceZhejiang University of TechnologyHangzhou 310014 People's Republic of China;
Key Laboratory of Pharmaceutical Engineering of Ministry of Education College of Pharmaceutical ScienceZhejiang University of TechnologyHangzhou 310014 People's Republic of China;
traceless directing group; C?H carbonylation; cobalt; benzylamine; (+)-garenoxacin;
机译:前封面图片:无痕指示组辅助钴催化的C?H苄胺的C?H羰基化(ADC。合成。催讯。2017年2月21日)
机译:前封面图片:氰醇(ETA(6) - 亚烯)卤化物(二齿膦)钌(II)复合物(ADC。合成。催留氰基)的无氰基醇脱氢
机译:前封面图片:氰醇(ETA(6) - 亚烯)卤化物(二齿膦)钌(II)复合物(ADC。合成。催留氰基)的无氰基醇脱氢
机译:封面:邻卤代苯酚和氰胺的羰基化-环化多米诺反应合成4H-苯并e 13恶嗪-4-酮(ChemistryOpen 5/2017)
机译:前封面图片:通过Ru催化的映选择性氢化的4-乙酰基的Multigram-Scalic Quicclophane:使用Planar和中枢性手性(Synth。Catal.12221)的ru-Catereded映选择性氢化:进入2.2截谱均匀(ADC。Catal。11/2021)