机译:铜催化供体-受体环丙烷对吲哚的高对映选择性环opentannulation
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China,Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;
Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China,Department of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China;
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;
机译:侧臂促进的高对映选择性开环反应和胺给体-受体环丙烷的动力学拆分
机译:简洁的吲哚衍生的供体 - 受体环丙烷的Pyrolizino [1,2-B]吲哚的方法
机译:吲哚衍生的供体-受体环丙烷的多米诺环二聚化:彭塔莱诺[1,6-a,b]吲哚骨架的一步构建
机译:3-取代吲哚的高度致力辅助氢化
机译:I.烯丙基醚的高度区域选择性非对映选择性定向加氢甲酰化。二。用于铜催化共轭加成的高度实用和对映选择性配体。
机译:供体 - 受体环丙烷的极性反转:通过不对称催化铱二取代δ内酯
机译:铜通过串联共轭加成-分子内烯醇盐捕集的反式-1-烷基-2-取代的环丙烷的铜催化对映选择性合成