迈克尔反应是一个典型的亲核加成反应，一直是有机化学领域的一个研究热点。
Michael reaction is a typical nucleophilic addition reaction, is always an organic chemistry domain research hot spot.
含活性基团的醛可与烯丙基碘和锡粉直接进行亲核加成反应，得到高烯丙基型的醇。水的存在不利于此反应的进行。
Aldehyde containing functional groups can react with allyl iodine and tin directly, water is of no advantage to the reaction.
本文比较了在甲醇介质下，2-苯基吲哚（1）单重态氧反应中的捕捉反应以及2-苯基-3H-吲哚-3-酮（4）的亲核加成反应特征。
Trapping reactions in singlet oxygenation of 2-phenylindole (1) and nucleophilic addition reactions of 2-phenyl-3H-indol-3-one (4) both in methanolic media were studied comparatively.
本文比较了在甲醇介质下，2-苯基吲哚（1）单重态氧反应中的捕捉反应以及2-苯基-3H-吲哚-3-酮（4）的亲核加成反应特征。
Trapping reactions in singlet oxygenation of 2-phenylindole (1) and nucleophilic addition reactions of 2-phenyl-3H-indol-3-one (4) both in methanolic media were studied comparatively.
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