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首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Construction of Azabicyclo[6.4.0]dodecatrienes Based on Rhodium(I)-Catalyzed Intramolecular [6+2] Cycloaddition between Azetidine, Allene, and Alkynes
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Construction of Azabicyclo[6.4.0]dodecatrienes Based on Rhodium(I)-Catalyzed Intramolecular [6+2] Cycloaddition between Azetidine, Allene, and Alkynes

机译:基于铑(I)催化的氮杂环丁烷,丙二烯和炔烃的分子内[6 + 2]环加成反应构建氮杂双[6.4.0]十二碳三烯

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摘要

Treatment of the allenylazetidine–alkynes with a catalytic amount of [RhCl(CO)dppp]2 (dppp: 1,3-bis(diphenylphosphino)propane) effected the intramolecular hetero-[6+2]-type ring-closing reaction via the C–C bond cleavage of the azetidine ring to produce azabicyclo[6.4.0]dodecatriene derivatives in good to excellent yields. The formation of the oxa analogue could also be achieved.
机译:用催化量的[RhCl(CO)dppp] 2 (dppp:1,3-双(二苯基膦基)丙烷)处理烯丙基氮杂环丁烷-炔烃可实现分子内杂-[6 + 2]-氮杂环丁烷环的C–C键裂解产生的A型双环闭合反应,可产生高至优异收率的氮杂双环[6.4.0]十二碳三烯衍生物。氧杂类似物的形成也可以实现。

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