Methanol as the C1source: Redox coupling of nitrobenzenes and alcohols for the synthesis of benzimidazoles
We present an operationally simple redox coupling for the synthesis of N-1 substituted benzimidazoles using feedstock building block 2-nitroaniline derivatives as the precursors and methanol as the C1 source. Higher atom, step, and redox economies and exc
An, Jie,Lai, Zemin,Li, Hengzhao,Peng, Mengqi,Sun, Yanhao,Yan, Zihan,Yang, Ruoyan,Zhang, Yuntong
supporting information
p. 748 - 753
(2022/02/02)
Cyclization of [(4- or 5-substituted-2-benzimidazolyl)thio]acetic acids. Isolation and identification of two possible isomers of substituted thiazolo[3,2-a]benzimidazol-3(2H)-one
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Tanaka,Ino,Murakami
p. 1876 - 1886
(2007/10/02)
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