Remarkably Efficient Synthesis of 2H-Indazole 1-Oxides and 2H-Indazoles via Tandem Carbon-Carbon Followed by Nitrogen-Nitrogen Bond Formation

被引:41
作者
Bouillon, Isabelle [1 ]
Zajicek, Jaroslav [1 ]
Pudelova, Nadezda [1 ]
Krchnak, Viktor [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Nieuwland Sci Ctr 251, Notre Dame, IN 46556 USA
关键词
D O I
10.1021/jo8018895
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Base-catalyzed tandem carbon-carbon followed by nitrogen-nitrogen bond formations quantitatively converted N-alkyl-2-nitro-N-(2-oxo-2-aryl-ethyl)-benzenesulfonamides to 2H-indazoles 1-oxides under mild conditions. Triphenylphosphine or mesyl chloride/triethylamine-mediated deoxygenation afforded 2H-indazoles.
引用
收藏
页码:9027 / 9032
页数:6
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