首页> 外文期刊>Journal of the Brazilian Chemical Society >Studies toward the synthesis of Amaryllidaceae alkaloids from Morita-Baylis-Hillman adducts. A straightforward synthesis of functionalized dihydroisoquinolin-5(6H)-one core
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Studies toward the synthesis of Amaryllidaceae alkaloids from Morita-Baylis-Hillman adducts. A straightforward synthesis of functionalized dihydroisoquinolin-5(6H)-one core

机译:从森田-贝利斯-希尔曼加合物合成金莲花科生物碱的研究。功能化二氢异喹啉5(6H)-一个核的直接合成

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摘要

We disclose herein our results concerning a study aiming at the synthesis of the highly substituted carbon skeleton of alkaloids isolated from plants of the Amaryllidaceae family. The total synthesis of the functionalized dihydroisoquinolin-5(6H)-one core, which is the bottom part of the structure of alkaloids isolated from this botanic family, is described, using Morita-Baylis-Hillman adducts as substrate. This compound should be a useful and valuable intermediate for the total synthesis of alkaloids isolated from Amaryllidaceae.
机译:我们在这里公开了我们的结果,该结果涉及旨在合成自芳科植物的生物碱的高度取代的碳骨架的研究。使用Morita-Baylis-Hillman加合物作为底物,描述了功能化的二氢异喹啉-5(6H)-一个核的总合成,该核是从该植物家族分离的生物碱结构的底部。该化合物应该是有用的和有价值的中间体,用于从金莲花科分离的生物碱的总合成。

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