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Trifluoroborane catalyzed chemoselective synthesis of highly functionalized 1,3‐thiazin‐2‐ylidenes
Journal of Heterocyclic Chemistry ( IF 2.0 ) Pub Date : 2020-07-16 , DOI: 10.1002/jhet.4049
Zhibin Luo 1 , Sangepu Bhavanarushi 1 , Avula Sreenivas 2 , Narra Srikanth Reddy 2 , Anil Valeru 1 , Imran Khan 1 , Yin Xu 1 , Bin Liu 1 , Jimin Xie 1
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An efficient chemoselective synthesis of 1,3‐thiazine‐2‐ylidenes was achieved via annulations of β‐aroyl‐thioacetamide with propargyl alcohols using BF3 OEt2 as Lewis acid catalyst. A broad spectrum of substrates was well tolerated under the mild reaction conditions producing desired thiazine heterocyclics in good yields.

中文翻译:

三氟硼烷催化化学合成高度官能化的1,3-噻嗪-2-亚烷基

使用BF 3 OEt 2作为路易斯酸催化剂,通过β-芳酰基-硫代乙酰胺与炔丙醇的环化反应,实现了1,3-噻嗪-2-亚基的高效化学选择性合成。在温和的反应条件下,广谱的底物具有良好的耐受性,能够以高收率产生所需的噻嗪杂环。
更新日期:2020-09-08
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