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首页> 外文期刊>New Journal of Chemistry >Hypervalent iodine catalysis for selective oxidation of Baylis-Hillman adducts via in situ generation of o-iodoxybenzoic acid (IBX) from 2-iodosobenzoic acid (IBA) in the presence of oxone
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Hypervalent iodine catalysis for selective oxidation of Baylis-Hillman adducts via in situ generation of o-iodoxybenzoic acid (IBX) from 2-iodosobenzoic acid (IBA) in the presence of oxone

机译:在己酮存在下通过从2-碘代苯甲酸(IBA)原位生成邻碘氧苯甲酸(IBX)的高价碘催化选择性氧化Baylis-Hillman加合物

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摘要

An efficient, environmentally benign, eco-friendly protocol for selective oxidation of primary and secondary Baylis-Hillman alcohols to the corresponding carbonyl compounds has been developed. We have demonstrated the catalytic use of o-iodoxybenzoic acid (IBX) generated in situ from 2-iodosobenzoic acid (IBA) in the presence of oxone (2KHSO(5)center dot KHSO4 center dot K2SO4) as a co-oxidant. This efficient method notably enables better to high yields without the use of any toxic heavy metals and the direct use of tricky IBX. Furthermore, the synthesized catalyst could be recovered conveniently using a reductive work-up.
机译:已经开发出一种有效的,对环境无害的,生态友好的方案,用于将伯利兹和伯利兹仲醇和仲醇选择性氧化为相应的羰基化合物。我们已经证明了在氧酮(2KHSO(5)中心点KHSO4中心点K2SO4)作为助氧化剂的存在下,从2-碘代苯甲酸(IBA)原位生成的邻碘氧苯甲酸(IBX)的催化用途。这种有效的方法尤其可以在不使用任何有毒重金属和直接使用棘手的IBX的情况下更好地提高产量。此外,可以通过还原后处理方便地回收合成的催化剂。

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