改变Fe2+当量的Minisci反应制备芳基吡啶甲醇的研究

IF 1.7 Q3 CHEMISTRY, ORGANIC
B. Özgeriş, F. Tümer
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引用次数: 0

摘要

我们的目标是合成羧酰胺8和10,然而,除了主要产物外,在反应溶液中还检测到一种物质。该副产物的表征表明它是主产物的另一种异构体。为了确定合成甲酰胺衍生物的反应条件,我们通过改变铁的化学计量进行了几个实验。当使用摩尔当量的Fe时,仅获得两个反应产物8和10。Fe化学计量的增加导致副产物9和11的形成,甚至通过Minisci反应形成还原的醇产物(12-15)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A study of Minisci reaction by changing Fe2+ equivalency: Preparation of arylpyridinyl methanol
We aimed the synthesis of carboxamide 8 and 10, however, beside the main product, one more species was detected in the reaction solution. The characterization of this side product showed that it was the other isomer of the main product. To establish reaction conditions for the synthesis of carboxamide derivatives, we have set up several experiments by changing the Fe stoichiometry. When a molar equivalent Fe was used, only two reaction products 8 and 10 were obtained. The increase in Fe stoichiometry caused the formation of side product 9 and 11 even formation of reduced alcohol products (12-15) by Minisci reaction.
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来源期刊
Organic Communications
Organic Communications CHEMISTRY, ORGANIC-
CiteScore
2.80
自引率
11.80%
发文量
21
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