Department of Organic Chemistry, University of Debrecen, H-4032 Debrecen, Egyetem tér 1., Hungary.
Chem Soc Rev. 2011 May;40(5):2797-847. doi: 10.1039/c0cs00101e. Epub 2011 Feb 17.
Organic azides are known and utilized in the synthetic organic chemistry as amine precursors, potential sources of nitrenes, dipoles useful in 1,3-dipolar cycloadditions and starting materials of phosphoranes for a long time, and their literature has been overviewed by several authors. On the other hand, there are some special subclasses within the azides which possess peculiar and interesting properties differing from those of the majority and offering extra synthetic possibilities. In this critical review we wish to give an exhaustive overview on the synthesis and synthetic potential of α-azido ketones and related systems, an underestimated group of compounds. The enhanced acidity of the α-hydrogen offers various new synthetic applications including the creation of a new C-C bond, while the joint presence of the carbonyl and vinyl functions of α-azido-α,β-unsaturated ketones results in a special reactivity, too. Chemo- and stereoselectivity issues also represent important points which are discussed in detail. Finally, the usefulness of the titled derivatives in the synthesis of various heterocycles is reviewed (273 references).
有机叠氮化物在合成有机化学中作为胺前体、氮烯的潜在来源、1,3-偶极环加成反应中有用的偶极子以及磷烷的起始材料已经被多位作者综述过。另一方面,叠氮化物中有一些特殊的子类,它们具有与大多数不同的特殊和有趣的性质,并提供额外的合成可能性。在这篇评论中,我们希望对α-叠氮酮和相关体系的合成和合成潜力进行全面概述,这是一组被低估的化合物。α-氢的增强酸性提供了各种新的合成应用,包括形成新的 C-C 键,而α-叠氮-α,β-不饱和酮的羰基和乙烯基功能的共同存在也导致了特殊的反应性。化学和立体选择性问题也是讨论的重点。最后,综述了标题衍生物在合成各种杂环中的有用性(273 个参考文献)。