PALLADIUM-CATALYZED COUPLING OF ACID CHLORIDES WITH ORGANOTIN REAGENTS

Palladium-Catalyzed Coupling of Acid Chlorides with Organotin Reagents (E)-Ethyl-4-(4-n1trophenyl)-4-oxo-2-butenoate A, F. Renaldo, J, W. Labadie, and J. K. Stille, Department of Chemistry, Colorado State University, Ft. Collins, CO 80523... [Pg.275]

Palladium, benzylchlorobis(triphenylphosphine)-, trans-, 67, 86 Palladium-catalyzed aryl-aryl coupling, 66, 70 PALLADIUM-CATALYZED ALLYLIC AMINATION, 67,105 PALLADIUM-CATALYZED CHLOROACETOXYLATION, 67, 105 PALLADIUM-CATALYZED COUPLING OF ACID CHLORIDES WITH ORGANOTIN REAGENTS, 67, 86 PALLADIUM-CATALYZED COUPLING OF ARYL HALIDES, 66, 67 PALLADIUM-CATALYZED syn-ADDITION OF CARBOXYLIC ACIDS,... [Pg.155]

PALLADIUM-CATALYZED COUPLING OF ACID CHLORIDES WITH ORGANOTIN REAGENTS ETHYL (E)-4-(4-NITR0-PHENYL)-4-0X0-2-BUTENOATE... [Pg.256]

Labadie JW, Stille JK (1983) Mechanisms of the palladium-catalyzed couplings of acid chlorides with organotin reagents. J Am Chem Soc 105 6129-6137... [Pg.82]

Prior to the studies which uncovered the utility of organotin acylation as described in the preceding paragraphs, acid chlorides were also found to undergo a similar rhodium(I)-mediated acylation with allyltins to form p, y-unsaturated ketones. The palladium(0)-catalyzed coupling has been found to be more general with respect to varied substitution patterns of both reagents and could be conducted under essentially neutral conditions (see Section 1.13.5.1). [Pg.438]

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