期刊
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
卷 39, 期 11, 页码 1660-1667出版社
MAIK NAUKA/INTERPERIODICA
DOI: 10.1023/B:RUJO.0000013144.15578.2d
关键词
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Conditions were found where in 6-halo-4-quinolines (halogen = iodine, bromine, or chlorine) the halo-en atoms were replaced in succession by similar or different aryl groups in cross-coupling reactions with arylboric acids catalyzed by palladium and nickel complexes. Basing on successive Suzuki reaction a convenient procedure was developed for preparation of diarylquinolines that did not require isolation of the intermediate monoarylation product and afforded almost quantitative yields of diarylquinolines.
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