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Org Biomol Chem ; 12(43): 8619-26, 2014 Nov 21.
Article in English | MEDLINE | ID: mdl-25231547

ABSTRACT

Cyclization-carbonylation of α,ß-alkynic hydrazones and (o-alkynylphenyl) (methoxymethyl) sulfides with Pd(tfa)2 in DMSO/MeOH afforded methyl pyrazole-4-carboxylates and benzo[b]thiophene-3-carboxylates, respectively, in good yields. A simple change of the ligand (solvent) allowed controlled, effective switching between cyclization-carbonylation-cyclization-coupling (CCC-coupling) reactions and cyclization-carbonylation reactions.


Subject(s)
Carboxylic Acids/chemical synthesis , Hydrazones/chemistry , Palladium/chemistry , Pyrazoles/chemical synthesis , Thiophenes/chemical synthesis , Catalysis , Cations, Divalent , Cyclization , Dimethyl Sulfoxide/chemistry , Ligands , Methanol/chemistry
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