化学
布洛芬
亲核细胞
组合化学
亲核加成
脚手架
立体化学
药物化学
催化作用
有机化学
药理学
计算机科学
医学
数据库
作者
Caifeng Yuan,Xuan-Rui Huang,Jian‐Hua Guo,Yiwen Shen,Na Shang,Qilin Tang,Jing Yang,Yi Huang,Hongbin Zhang,E Tang
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-06-06
卷期号:26 (23): 4992-4997
标识
DOI:10.1021/acs.orglett.4c01655
摘要
A metal-free and mild approach for constructing 5-amino-1,2-selenazole skeletons by NBS/KSeCN-mediated N-selenocyanation and nucleophilic cyclization of β-enaminones has been developed. Various isoselenazole compounds and the isoselenazolyl derivatives of anti-inflammatory medicines, including isosepac, oxaprozin, and ibuprofen, have been obtained with good yields. This efficient, "one-pot", and atomic economy strategy may represent an alternative route for the construction of a 1,2-selenazole framework via the "+SeCN" pathway and provide new access to heterocycles containing a Se–N bond.
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