Reference

Synthesis of aryl esters by palladium catalyzed carbonylation of aryl iodides

Synthesis of aryl esters by palladium catalyzed carbonylation of aryl iodides. Nikitin, K. V.; Andryukhova, N. P.; Bumagin, N. A.; Beletskaya, I. P. (M. V. Lomonosov Moscow State Univ., Moscow 119899, USSR). Mendeleev Commun., (4), 129-31 (English) 1991. 5029-67-4 is the cas registry number of certain chemical which is used as reagents here. CODEN: MENCEX. 5029-67-4 which is the cas registry number of some chemical is mentioned. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) Optimal conditions for the title reactions included 0.5 mol % Pd(OAc)2 as catalyst, DMF as solvent, 1 atm CO, NaOH as base, and a small excess of phenol. Phosphine ligands in the catalyst retarded the reaction. Yields of 385% were obtained in some cases, e.g., BzOC6H4R-4 (R = H, OMe) and Ph 2-naphthoate. ..

Synthesis of aryl esters by palladium catalyzed carbonylation of aryl iodides

Synthesis of aryl esters by palladium catalyzed carbonylation of aryl iodides. Nikitin, K. V.; Andryukhova, N. P.; Bumagin, N. A.; Beletskaya, I. P. (M. V. Lomonosov Moscow State Univ., Moscow 119899, USSR). Mendeleev Commun., (4), 129-31 (English) 1991. 5029-67-4 is the cas registry number of certain chemical which is used as reagents here. CODEN: MENCEX. 5029-67-4 which is the cas registry number of some chemical is mentioned. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) Optimal conditions for the title reactions included 0.5 mol % Pd(OAc)2 as catalyst, DMF as solvent, 1 atm CO, NaOH as base, and a small excess of phenol. Phosphine ligands in the catalyst retarded the reaction. Yields of 385% were obtained in some cases, e.g., BzOC6H4R-4 (R = H, OMe) and Ph 2-naphthoate. ..