醇盐
化学
氢氧化物
亲核细胞
胺气处理
选择性
吲唑
基质(水族馆)
亲核加成
组合化学
药物化学
无机化学
有机化学
催化作用
海洋学
地质学
作者
Jie S. Zhu,Matthew R. Duong,Andrew P. Teuthorn,Julia Y. Lu,Jung-Ho Son,Makhluf J. Haddadin,Mark J. Kurth
标识
DOI:10.1021/acs.orglett.8b00036
摘要
Reaction options, alkoxide vs hydroxide vs amine addition to the key intermediate (o-nitrosoimine) generated in the Davis-Beirut reaction of an o-nitrobenzylamine substrate, are reported to explain the nucleophilic addition selectivity of this one-pot indazole-forming process. The hydroxide addition/deprotection pathway as well as the fate of the resulting o-nitrosobenzaldehyde were both uncovered with several o-nitrobenzylamine substrates, and design elements required for an efficient double Davis-Beirut reaction, inspired by new mechanistic insights, were defined.
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