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Site-Selective Suzuki–Miyaura Reaction of 6,8-Dichloro-1,2,4-triazolo[4,3-a]pyridines
Synlett ( IF 1.7 ) Pub Date : 2020-06-03 , DOI: 10.1055/s-0040-1707138
Peter Langer 1, 2 , David Kuhrt 1, 2 , Peter Ehlers 1, 2 , Anke Spannenberg 2
Affiliation  

Triazolopyridines have found various applications as pharmaceuticals, agrochemicals, or optical materials. Consequently, the introduction of various functionalities at specific sites of this heterocyclic framework is of great importance. In this regard, we report the development of a site-selective Suzuki–Miyaura reactions leading to substituted triazolopyridines at positions 6 and 8. Under optimized conditions, the respective products have been obtained with high selectivity and yield.

中文翻译:

6,8-二氯-1,2,4-三唑并[4,3-a]吡啶的位点选择性铃木-宫浦反应

三唑并吡啶已发现作为药物、农用化学品或光学材料的各种应用。因此,在该杂环骨架的特定位点引入各种功能非常重要。在这方面,我们报告了位点选择性 Suzuki-Miyaura 反应的发展,导致在位置 6 和 8 处被取代的三唑并吡啶。在优化条件下,以高选择性和高产率获得了相应的产物。
更新日期:2020-06-03
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