BF3‧OEt2 促进从(苯乙炔基)-芴和 2-肼基吡啶衍生物合成 9-亚芴基 2-肼基吡啶亚胺的过程

IF 1.8 3区 化学 Q3 CHEMISTRY, ORGANIC
Suresh Snoxma Smile , Harichandran Gurusamy , Ponnusamy Shanmugam
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引用次数: 0

摘要

以BF3-OEt2为路易斯酸催化剂,使9-芴丙炔醇与取代的2-肼基吡啶反应,得到9-芴亚甲基2-肼基吡啶亚胺衍生物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BF3‧OEt2 promoted synthesis of 9-fluorenlidene appended 2-hydrazinopyridine imines from (phenylethynyl)-fluorene and 2-hydrazinopyridine derivatives

Reaction of 9-fluorene propargylic alcohols and substituted-2-hydrazinopyridine using BF3·OEt2 as a Lewis acid catalyst afforded 9-fluorenlidene appended 2-hydrazinopyridine imine derivatives has been developed. The scope of the reaction is demonstrated by selecting a range of fluorene propargylic alcohols and substituted 2-hydrazinopyridine imines. All the synthesized molecules were characterized using various spectroscopic and analytical techniques including 1H NMR,13C NMR, and Mass spectrometry. A plausible reaction mechanism for forming title compounds via propargylic allenyl carbocation is postulated. The synthetic utility of products thus formed is demonstrated by utilizing Suzuki coupling.

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来源期刊
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
期刊介绍: Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.
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