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Synthesis of furo[2,3-b]pyridine
Journal of Heterocyclic Chemistry ( IF 2.0 ) Pub Date : October 1971 , DOI: 10.1002/jhet.5570080509 J. W. Mcfarland , R. P. Wollerman , W. C. Sadler , G. N. Coleman
Journal of Heterocyclic Chemistry ( IF 2.0 ) Pub Date : October 1971 , DOI: 10.1002/jhet.5570080509 J. W. Mcfarland , R. P. Wollerman , W. C. Sadler , G. N. Coleman
Two routes were employed to synthesize unsubstituted furo[2,3-b]pyridine (IV). The first method started with ethyl 5-aminofuro[2,3-b] pyridine-2-carboxylate (1) and involved successive deamination, hydrolysis, and decarboxylation. The second method began with 5-nitrofuro[2,3-b ]-pyridine-2-carboxylic acid (V) and consisted of successive decarboxylation, reduction, and deamination reactions.
中文翻译:
呋喃并[2,3- b ]吡啶的合成
采用两种途径合成未取代的呋喃并[2,3- b ]吡啶(IV)。第一种方法始于5-氨基呋喃[2,3- b ]吡啶-2-羧酸乙酯(1),包括连续的脱氨基,水解和脱羧作用。第二种方法以5-硝基呋喃并[2,3- b ]-吡啶-2-羧酸(V)开始,由连续的脱羧,还原和脱氨基反应组成。
更新日期:2017-01-31
中文翻译:
![](https://scdn.x-mol.com/jcss/images/paperTranslation.png)
呋喃并[2,3- b ]吡啶的合成
采用两种途径合成未取代的呋喃并[2,3- b ]吡啶(IV)。第一种方法始于5-氨基呋喃[2,3- b ]吡啶-2-羧酸乙酯(1),包括连续的脱氨基,水解和脱羧作用。第二种方法以5-硝基呋喃并[2,3- b ]-吡啶-2-羧酸(V)开始,由连续的脱羧,还原和脱氨基反应组成。