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Synthesis of indoles: recent advances

机译:吲哚的综合:最近的进展

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Published data of the last 10 years concerning the development of new and upgrading of known approaches to indole synthesis are integrated and analyzed. Modern versions of the classical syntheses such as the Fischer synthesis, Nenitzescu synthesis, Ullmann reaction, Leimgruber-Batcho synthesis, Reissert synthesis, Bartoli reaction, Madelung synthesis and Cadogan-Sundberg reaction are considered. The presented new approaches include transformations of heterocycles, synthesis from o-alkynylanilines, reductive cyclization of nitrobenzene derivatives, synthesis with the use of arynes and catalysis by N-heterocyclic carbenes. The final Section summarizes original methods for the synthesis of indoles other than those listed above; they are classified in terms of the nature of the forming bond (C-C, C-N). Rarely used methods based on benzene ring construction in pyrrole derivatives are discussed separately.
机译:综合和分析了关于开发已知吲哚合成的已知方法的新的和升级新的和升级的最近10年的数据。 考虑了现代版本的古典合成,如Fischer合成,Nenitzescu合成,Ullmann反应,Leimgruber-Batcho合成,Reissert合成,Bartoli反应,Madelung合成和Cadogan-Sundberg反应。 所提出的新方法包括杂环的转化,由O-炔基胺的合成,硝基苯衍生物的还原环化,合成通过使用芳香剂和催化通过N-杂环碳酸催化。 最终部分总结了合成上述人员以外的识别的原始方法; 它们以成形键(C-C,C-N)的性质为分类。 很少使用基于吡咯衍生物中的苯环结构的方法进行单独讨论。

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