首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS OF PHENYLSELANYLISOCHROMAN-1-ONES THROUGH HIGHLY SELECTIVE SELENOLACTONIZATION OF STYRENE-TYPED CARBOXYLIC ACIDS
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SYNTHESIS OF PHENYLSELANYLISOCHROMAN-1-ONES THROUGH HIGHLY SELECTIVE SELENOLACTONIZATION OF STYRENE-TYPED CARBOXYLIC ACIDS

机译:苯乙烯型羧酸的高选择性亚硒化合成苯并三异氰酸酯-1-酮

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摘要

The novel synthesis of phenylselanylisochroman-1-ones was achieved by selenolactonization of styrene-typed carboxylic acids and phenylselenenyl chloride in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO). The reactions give excellent yields with high exo-selectivity.
机译:在1,4-二氮杂双环[2.2.2]辛烷(DABCO)存在下,苯乙烯型羧酸和苯基硒烯基氯的烯内酯化可以实现苯基硒基异色满-1-酮的新型合成。该反应具有高的选择性和高的产率。

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