palladium diacetate; toluene-4-sulfonic acid; triphenylphosphine in dichloromethane T=100°C; P=20685.9 Torr; 48 h;

palladium diacetate; toluene-4-sulfonic acid; triphenylphosphine in dichloromethane T=100 - 120°C; P=20685.9 Torr; 48 h; further reagents and conditions;

palladium diacetate; triphenylphosphine in dichloromethane T=100°C; P=2068.6 Torr; 5 h;

palladium diacetate; triphenylphosphine in dichloromethane T=100°C; P=2068.6 Torr; 8 h;

palladium diacetate; triphenylphosphine in dichloromethane T=110°C; Carbonylation; thiolysis; P=20686.5 Torr; 60 h;

toluene-4-sulfonic acid; triphenylphosphine; palladium diacetate in tetrahydrofuran T=100°C; P=20685.9 Torr; 48 h; Yields of byproduct given;

palladium diacetate; triphenylphosphine in tetrahydrofuran T=100°C; P=20685.9 Torr; 48 h; other allenes, other thiols, other reagents: Pd(PPh3)4, Pd(OAc)2, Pd(OAc)2/dppp, Pd(OAc)2/dppb, other Pd, Ru and Rh complexes, Co2(CO)8, other solvents: DME, CH2Cl2, C6H6, various reactants ratio, other pressure, other temperature and reaction time; MechanismProduct distribution;

palladium diacetate; 1,4-di(diphenylphosphino)-butane in dichloromethane T=110°C; Carbonylation; thiolysis; P=20686.5 Torr; 60 h; Product distribution; Further Variations:ReagentsSolventsreaction time;

in N,N-dimethyl-formamide T=70°C; Yield given. Yields of byproduct given;