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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >UNEXPECTED FORMATION OF 4,7-DIHALOBENZObTHIOPHENES USING OHIRA-BESTMANN REAGENT AND REACTIVITY OF THE HALOGEN-SUBSTITUTED BENZObTHIOPHENES IN SUZUKI-MIYAURA COUPLING WITH PHENYLBORONIC ACID
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UNEXPECTED FORMATION OF 4,7-DIHALOBENZObTHIOPHENES USING OHIRA-BESTMANN REAGENT AND REACTIVITY OF THE HALOGEN-SUBSTITUTED BENZObTHIOPHENES IN SUZUKI-MIYAURA COUPLING WITH PHENYLBORONIC ACID

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摘要

Reaction of 2-(1-adamantylsulfany1)-3,6-dihalobenzaldehydes with Ohira-Bestmann reagent gave 4,7-dihalobenzobthiophenes along with normal alkyne products. Nine types of 4,7-dihalobenzobthiophenes bearing chlorine, bromine, or iodine atoms, were prepared by this method. Regioselectivity in Suzuki-Miyaura cross coupling reactions of the 4,7-dihalobenzobthiophenes with PhB(OH)(2) was also studied.

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