ABSTRACT
They all fall down: The value of domino processes can be greatly enhanced when the possibility exists for one to selectively diverge from a common intermediate. In preliminary studies the dual reactivity of aryl-palladium intermediates is exploited. A diverse array of fluorene and phenanthrene derivatives were synthesized in a rapid and efficient manner (see scheme).
Subject(s)
Fluorenes/chemistry , Palladium/chemistry , Phenanthrenes/chemistry , Catalysis , Fluorenes/chemical synthesis , Phenanthrenes/chemical synthesis , StereoisomerismABSTRACT
A palladium-catalyzed C-H functionalization reaction for the synthesis of highly substituted aromatic nitriles is reported. The modularity of the reaction is demonstrated by the broad range of aryl iodides which can be coupled with metal cyanides and alkyl halides or aryl bromides.
Subject(s)
Benzene Derivatives/chemical synthesis , Nitriles/chemical synthesis , Palladium/chemistry , Alkylation , Benzene Derivatives/chemistry , Hydrocarbons, Halogenated/chemistry , Nitriles/chemistry , Norbornanes/chemistryABSTRACT
A norbornene-mediated palladium-catalyzed tandem alkylation/cyanation sequence is described in which an alkyl-aryl bond and a nitrile-aryl bond are formed in one pot. A variety of sterically hindered, five-, six-, and seven-membered ring benzonitriles were synthesized in good yields from easily accessible starting materials.
ABSTRACT
A variety of di- and trisubstituted thiophenes were synthesized by a one-pot palladium-catalyzed ortho-alkylation sequence terminated by either Heck or C-H coupling. Initial results toward the functionalization of indoles are also presented.
ABSTRACT
[reaction: see text] A palladium-catalyzed arylation of allylic acetates followed by beta-acetoxy elimination was shown to produce Heck-type coupling products. Optimal reaction conditions employed ligand-free palladium on carbon in the presence of tetrabutylammonium chloride, a trialkylamine base, and water.
