Polystyrene supported thiopseudourea Pd(II) complex: Applications for Sonogashira, Suzuki-Miyaura, Heck, Hiyama and Larock heteroannulation reactions

A highly active recyclable gold–graphene nanocomposite material for oxidative esterification and Suzuki cross-coupling reactions in green pathway

“…Table 5 provides a comparison of the results obtained for our present catalytic system with those reported in the literature [45][46][47][48]. From Table 5, it is seen that Au-G nanocomposite showed higher catalytic activity over these catalysts.…”

Polymer‐supported palladium (II) containing N2O2: An efficient and robust heterogeneous catalyst for C–C coupling reactions

“…For example, SMNPs‐salen Pd(II) needed longer time for the model reaction, and the temperature was high. Furthermore, a higher yield (97%) was obtained than that of PS‐tsu‐Pd(II) (92%), and the time was shorter than the case of Fe 3 O 4 /P(GMA‐AA‐MMA)‐Schiff base‐Pd . The TbPo‐Pd(II) is a promising candidate showing excellent catalytic activity in short time and low temperature.…”

Palladium-Catalyzed Denitrative Mizoroki–Heck Reaction

“…1,137.0,134.8,130.3,129.3,127.5,127.2,126.5,126.1,114.0,55.2,21.2;HRMS (DART) (E)-1-Methoxy-3-(4-methylstyryl)benzene (3Ae) [22] Purification by PTLC (hexane/CH2Cl2 = 1:1) afforded 3Ae as a yellow solid (27.0 mg, 60% yield). 8, 138.9, 137.6, 134.4, 129.6, 129.4, 128.9, 127.5, 126.4, 119.1, 113.1, 111.6, 55.2, 21.2 (E)-1-Methoxy-2-(4-methylstyryl)benzene (3Af) [23] Purification by PTLC (hexane/CH2Cl2 = 2:1) afforded 3Af as a white solid (32.1 mg, 72% yield). 7, 137.2, 135.1, 129.3, 129.0, 128.4, 126.5, 126.4, 126.2, 122.3, 120.7, 110.8, 55.4, 21.2 N,N-Dimethyl-4-(4-methylstyryl)aniline (3Ag) [24] Purification by PTLC (hexane/CH2Cl2 = 2:1) afforded 3Ag as a white solid (34.6 mg, 73% yield).…”