3-Iodo-4-chalcogen-2H-benzopyran as a convenient precursor for the sonogashira cross-coupling: synthesis of 3-alkynyl-4-chalcogen-2H-benzopyrans |
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Authors: | Adriane Speranç a |
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Affiliation: | Laboratório de Síntese, Reatividade, Avaliação Farmacológica e Toxicidade de Organocalcogênios, CCNE, UFSM, Santa Maria, Rio Grande do Sul CEP 97105-900, Brazil |
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Abstract: | 3-Iodo-4-chalcogen-2H-benzopyran derivatives underwent a direct Sonogashira cross-coupling reaction with several terminal alkynes in the presence of a catalytic amount of Pd(PPh3)2Cl2 with CuI as a co-catalyst, using Et3N as base and solvent. This cross-coupling reaction proceeded cleanly under mild conditions and was performed with propargylic alcohols, propargylic ethers, as well as alkyl and aryl alkynes, furnishing the correspondent 3-alkynyl-4-chalcogen-2H-benzopyrans in good yields. |
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Keywords: | Benzopyrans Palladium Sonogashira cross-coupling |
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