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Biaryl-2-thiols

Microwave and fluorous technologies have been combined in the solution phase parallel synthesis of 3-aminoimidazo[l,2-a]pyridines and -pyrazines [63]. The three-component condensation of a perfluorooctane-sulfonyl (Rfs = CgFiy) substituted benzaldehyde by microwave irradiation in a single-mode instrument at 150 °C for 10 min in CH2CI2 - MeOH in the presence of Sc(OTf)3 gave the imidazo-annulated heterocycles that could be purified by fluorous solid phase extraction (Scheme 9). Subsequent Pd-catalyzed cross-coupling reactions of the fluorous sulfonates with arylboronic acids or thiols gave biaryls or aryl sulfides, respectively, albeit it in relatively low yields. [Pg.40]


See other pages where Biaryl-2-thiols is mentioned: [Pg.332]    [Pg.75]    [Pg.2309]    [Pg.173]    [Pg.1754]    [Pg.138]    [Pg.332]    [Pg.12]    [Pg.492]   
See also in sourсe #XX -- [ Pg.332 ]




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