首页> 外文期刊>The Journal of Organic Chemistry >DMAP-catalyzed [3 + 2] and [4 + 2] cycloaddition reactions between [60]fullerene and unmodified Morita-Baylis-Hillman adducts in the presence of Ac_2O
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DMAP-catalyzed [3 + 2] and [4 + 2] cycloaddition reactions between [60]fullerene and unmodified Morita-Baylis-Hillman adducts in the presence of Ac_2O

机译:在Ac_2O存在下[60]富勒烯与未修饰的Morita-Baylis-Hillman加合物之间DMAP催化的[3 + 2]和[4 + 2]环加成反应

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摘要

One-step DMAP-catalyzed [3 + 2] and [4 + 2] cycloaddition reactions between C_(60) and unmodified Morita-Baylis-Hillman adducts in the presence of Ac_2O have been developed for the easy preparation of cyclopentene- and cyclohexene-fused [60]fullerene derivatives. When the MBH adducts bear an alkyl group, two different reaction pathways could be controlled selectively depending on the conditions.
机译:在Ac_2O存在下,C_(60)与未修饰的Morita-Baylis-Hillman加合物之间的单步DMAP催化[3 + 2]和[4 + 2]环加成反应已经开发出来,可轻松制备环戊烯和环己烯。稠合的[60]富勒烯衍生物。当MBH加合物带有烷基时,可以根据条件选择性控制两个不同的反应路径。

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