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。
Methods tropisetron hydrochloride was synthesized from indol-3-yl carboxylic acid by chlorination and condensation with tropic alcohol lithium, then salt formation with hydrochlororic acid.
方法：以吲哚-3-甲酸为起始原料，酰氯化后与托品醇锂发生缩合反应，再与盐酸成盐制得盐酸托烷司琼。
Unsymmetrical bisindolylalkane with 73%~99% of yields were synthesized by iodine catalyzation from indole with(1H-indol-3-yl)(alkyl)methanol under solvent free condition at room temperature.
在室温以及无溶剂条件下，吲哚与烷基-3-吲哚基甲醇在碘的催化下以73%~99%的高收率得到不对称双吲哚烷基化合物。
Unsymmetrical bisindolylalkane with 73%~99% of yields were synthesized by iodine catalyzation from indole with(1H-indol-3-yl)(alkyl)methanol under solvent free condition at room temperature.
在室温以及无溶剂条件下，吲哚与烷基-3-吲哚基甲醇在碘的催化下以73%~99%的高收率得到不对称双吲哚烷基化合物。
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