首页> 外文期刊>Chemistry: A European journal >Synthesis of 11-cis-retinoids by hydrosilylation-protodesilylation of an 11,12-didehydro precursor: Easy access to 11- and 12-mono- and 11,12-dideuteroretinoids
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Synthesis of 11-cis-retinoids by hydrosilylation-protodesilylation of an 11,12-didehydro precursor: Easy access to 11- and 12-mono- and 11,12-dideuteroretinoids

机译:通过11,12-二氢氢化物的氢化硅烷化-去甲硅烷基化反应合成11-顺-维甲酸:容易获得11-和12-单-和11,12-二氢类维甲酸

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摘要

An expeditious, highly efficient approach to 11-cis-retinoids was achieved by semihydrogenation of a readily available 11-yne precursor through a hydrosilylation-protodesilylation protocol. The complete chemo-, regio-, and syn-stereoselectivity of the method also allowed direct access to 11- and 12-monodeutero-, and 11,12-dideutero-11-cis-retinoids. The analogous trans series was not accessible by this route, and was synthesized by means of Hiyama coupling.
机译:一种快速,高效的11-顺-类视黄醇方法是通过氢化硅烷化-原去甲硅烷基化方案对易于获得的11-炔前体进行半氢化而实现的。该方法具有完全的化学,区域和顺式立体选择性,还可以直接进入11-和12-单十二烷基和11,12-二十二烷基-十一-类视黄醇。通过该途径无法获得类似的反式序列,并且是通过Hiyama耦合合成的。

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