化学
小学(天文学)
吲唑
烷基
反应性(心理学)
组合化学
酒
功能群
药物化学
有机化学
天文
医学
物理
病理
替代医学
聚合物
作者
Jie S. Zhu,Niklas Kraemer,Marina E. Shatskikh,Clarabella J. Li,Jung‐Ho Son,Makhluf J. Haddadin,Dean J. Tantillo,Mark J. Kurth
出处
期刊:Organic Letters
[American Chemical Society]
日期:2018-08-01
卷期号:20 (16): 4736-4739
被引量:29
标识
DOI:10.1021/acs.orglett.8b01655
摘要
A concise, one-step route to indazolones from primary alkyl amines and o-nitrobenzyl alcohols is reported. The key step in this readily scalable indazolone forming process involves base-mediated in situ o-nitrobenzyl alcohol → o-nitrosobenzaldehyde conversion. Although this functional group interconversion is known to be useful for 2H-indazole synthesis, its reactivity was modulated for indazolone formation.
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