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无溶剂条件下高速球磨中的交叉脱氢偶联反应在功能化四氢异喹啉合成中的应用。

Solvent-free cross-dehydrogenative coupling reactions under high speed ball-milling conditions applied to the synthesis of functionalized tetrahydroisoquinolines.

机构信息

Key Laboratory of Pharmaceutical Engineering of Ministry of Education, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, PR China.

出版信息

J Org Chem. 2011 Nov 4;76(21):9144-50. doi: 10.1021/jo2015533. Epub 2011 Oct 12.

Abstract

Solvent-free reaction using a high-speed ball milling technique has been first applied to cross-dehydrogenative coupling (CDC) reactions between tetrahydroisoquinolines and three types of pronucleophiles such as nitroalkanes, alkynes, and indoles. All coupling products were obtained in good yields at short reaction times (no more than 40 min). When alkynes and indoles were used as pronucleophile, the reactions can be catalyzed efficiently by recoverable copper balls without any additional metal catalyst.

摘要

无溶剂反应采用高速球磨技术,首次应用于四氢异喹啉与三种类型的亲核试剂(如硝基烷烃、炔烃和吲哚)之间的交叉脱氢偶联(CDC)反应。所有偶联产物均在较短的反应时间(不超过 40 分钟)内以良好的收率获得。当炔烃和吲哚作为亲核试剂时,反应可以在可回收的铜球的催化下高效进行,而无需任何额外的金属催化剂。

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