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三氟甲磺酸银催化的 1-((2-对甲苯磺酰氨基)芳基)丁-2-炔-1,4-二醇的串联杂环化/炔基化反应生成 2-炔基吲哚。

Silver triflate catalyzed tandem heterocyclization/alkynylation of 1-((2-tosylamino)aryl)but-2-yne-1,4-diols to 2-alkynyl indoles.

机构信息

Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.

出版信息

Chemistry. 2012 May 14;18(20):6133-7. doi: 10.1002/chem.201200578. Epub 2012 Apr 18.

Abstract

Don't cross me! 2-Alkynyl indoles were prepared efficiently by the AgOTf-catalyzed tandem heterocyclization/alkynylation of 1-(2-tosylamino)aryl)but-2-yne-1,4-diols under mild conditions (see scheme). The attractiveness of this approach lies in the fact that both the indole ring and alkyne side chain of the N-heterocycle are sequentially formed from low cost, readily available, and ecologically benign starting materials. It also provides the first route to this synthetically valuable class of compounds that is not based on a cross-coupling strategy.

摘要

别惹我!AgOTf 催化的温和条件下,1-(2-对甲苯磺酰氨基)芳基)-2-炔基-1,4-二醇的串联杂环化/炔基化反应可以高效制备 2-炔基吲哚(见方案)。这种方法的吸引力在于,吲哚环和 N-杂环的炔基侧链都是由成本低、易得且环境友好的起始原料依次形成的。这也为这一类具有合成价值的化合物提供了第一条非基于交叉偶联策略的合成路线。

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