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Ag(I)-Catalyzed one-pot synthesis of 4-fluorobenzo[b][1,6] naphthyridines and 4-fluoroisoquinolines via iminofluorination of alkynes with Selectfluor
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2017-06-19 00:00:00 , DOI: 10.1039/c7qo00346c
Kalpana Mishra 1, 2, 3, 4, 5 , Jay Bahadur Singh 1, 2, 3, 4, 5 , Tanu Gupta 1, 2, 3, 4, 5 , Radhey M. Singh 1, 2, 3, 4, 5
Affiliation  

Ag(I)-Catalyzed one-pot synthesis of 4-fluorobenzo[b][1,6]naphthyridines is described from o-alkynylquinolinyl aldehydes through imines in good to excellent yields. Selectfluor is used as a fluorinating reagent and the reaction proceeded at room temperature in an open atmosphere. Reactions employed in this synthesis method are also applied for the synthesis of 8-fluoro-1,6-naphthyridine, 7-fluoro-pyrazolo[4,3-c]pyridine and 4-fluoroisoquinoline derivatives. Standardized conditions were also applied on a gram scale reaction and gave a good yield of the product.

中文翻译:

银()4-氟苯并[ -催化的单罐合成b ] [1,6]萘啶和4- fluoroisoquinolines经由与的Selectfluor炔烃的iminofluorination

邻-炔基喹啉基醛到亚胺,以良好或极好的产率描述了Ag(I)催化的4-氟苯并[ b ] [1,6]萘啶的一锅合成。Selectfluor用作氟化剂,反应在室温下在开放气氛下进行。在该合成方法中采用的反应也用于合成8-氟-1,6-萘吡啶,7-氟-吡唑并[4,3- c ]吡啶和4-氟异喹啉衍生物。标准化条件也用于克规模的反应,并给出了良好的产物收率。
更新日期:2017-08-23
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