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Part I: Nitroalkenes in the synthesis of heterocyclic compounds

机译:第一部分:硝基烯烃在杂环化合物的合成中

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摘要

The applications of nitroalkenes in the synthesis of three- to five-membered O, N and S-heterocycles, including natural products are investigated in this review. These heterocyclic compounds were synthesized from nitroalkenes with a variety of substituents at the alpha and beta-positions and those that were part of common and medium rings via a wide variety of reactions such as Michael addition reactions, epoxidation, [3 + 2] cycloaddition and many cascade/domino/tandem reactions. In addition, the potential of nitroalkenes to take part in multi-component and cascade reactions, particularly, in diastereo- and enantioselective versions is reviewed. The high reactivity of nitroalkenes and their potential to coordinate with the metal catalysts as well as organocatalysts signify them as efficient precursors in synthetic organic chemistry. Also, the flexibility of the nitro group in functional group manipulations has expanded the scope of the nitro group, in general, and nitroalkenes, in particular, in organic synthesis.
机译:本文综述了硝基烯烃在三元至五元O,N和S杂环(包括天然产物)合成中的应用。这些杂环化合物是由硝基烯烃合成的,它们在α和β位置具有多个取代基,并且是通过常见的反应(例如迈克尔加成反应,环氧化,[3 + 2]环加成和许多级联/多米诺/串联反应。另外,综述了硝基烯烃参与多组分和级联反应的潜力,特别是在非对映和对映选择性形式中的潜力。硝基烯烃的高反应活性及其与金属催化剂和有机催化剂配位的潜力表明它们是合成有机化学中有效的前体。同样,在官能团操作中,硝基的柔韧性通常扩大了硝基的范围,尤其是有机合成中,尤其是硝基烯烃的范围。

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