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机译:N-苄基(ThiO)酰胺的电化学分子内脱氢偶联:直接和容易合成4H-1,3-苯并恶嗪和4H-1,3-苯并噻嗪
School of Chemical Science and Engineering Shanghai Key Lab of Chemical Assessment and Substainability Tongji University 1239 Siping Road Shanghai 200092 P. R. China;
School of Chemical Science and Engineering Shanghai Key Lab of Chemical Assessment and Substainability Tongji University 1239 Siping Road Shanghai 200092 P. R. China;
School of Chemical Science and Engineering Shanghai Key Lab of Chemical Assessment and Substainability Tongji University 1239 Siping Road Shanghai 200092 P. R. China;
School of Chemical Science and Engineering Shanghai Key Lab of Chemical Assessment and Substainability Tongji University 1239 Siping Road Shanghai 200092 P. R. China;
Electrochemistry; Intramolecular dehydrogenative coupling; Amides; Cyclization;
机译:N-苄基(ThiO)酰胺的电化学分子内脱氢偶联:直接和容易合成4H-1,3-苯并恶嗪和4H-1,3-苯并噻嗪
机译:通过金属和氧化试剂游离芳族C-H氧合合成4H-1,3-苯并恶嗪
机译:在无金属条件下硫酰胺的分子内脱氢C-S键偶联形成1,3-苯并噻嗪
机译:通过SPC的无烷基膦氧化物的无晶体直接合成钯αH/ p(O)αH/ p(O)αH脱氢偶联
机译:1.通过原位生成的Schwartz试剂(Cp2氯化锆(氢)氯化物)将叔苄酰胺还原为苯甲醛;麦角酸的正式合成。 2. Ru催化的酰胺基芳烃碳氢,碳氮和碳氧键功能化:C-B形成,碳-碳铃木交叉偶联和加氢脱甲氧基化
机译:通过sp2 C–H和sp3 C–H键的无过渡金属分子内脱氢偶联(IDC)合成2-氧吲哚
机译:双((4-R-5-(噻吩-2-基甲基)-4H-1,2,4-三唑-3-基-3-基)的合成和性质)硫醇