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Easy Access to Polyfunctionalized Chiral Decalins

机译:轻松进入多官能化手性划分蛋白

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摘要

An unexpected ring expansion that converts hydrindanes into decalins via an unprecedented dyotropic reaction involving a mesylate group has been observed, and this paved the way for easy access to polyfunctionalized chiral decalins. These polyfunctionalized chiral decalins can be very useful building blocks for the synthesis of the thia analogues of many natural compounds. They can also be used in asymmetric catalysis and also in the synthesis of the new analogues of vitamin D with a modified D ring and side chain. The use of chiral sulfoxide ligands for asymmetric catalysis or asymmetric sulfur ylide-mediated epoxidation of carbonyl compounds is a very important topic in the field of organic chemistry, hence our results could be useful to the scientific community.
机译:已经观察到通过前所未有的涉及甲磺酸盐基团的前所未有的尿素反应将水吲哚转化为癸烯的意外的环形膨胀,并且这铺设了方便进入多官能化手性癸苯胺。这些多官能化手性癸蛋白可以是非常有用的构建块,用于合成许多天然化合物的类似物。它们还可用于不对称催化,也可以在合成维生素D的新类似物与改性的D环和侧链。使用手性亚砜配体进行不对称催化或不对称硫的亚氧化羰介导的羰基化合物的环氧化是有机化学领域的一个非常重要的话题,因此我们的结果对于科学界可能有用。

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