Synthesis of Benzimidazolones via One-Pot Reaction of Hydroxylamines, Aldehydes, and Trimethylsilyl Cyanide Promoted by Diacetoxyiodobenzene
Author:
Affiliation:
1. College of Chemistry and Chemical Engineering, Northwest Normal University, 967 Anning East Road, Lanzhou 730070, P. R. China
2. State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. China
Funder
National Natural Science Foundation of China
Key Laboratory Polymer Materials of Gansu Province, Northwest Normal University
Bioactive Product Engineering Research Center for Gansu Distinctive Plants
State Key Laboratory of Applied Organic Chemistry, Lanzhou University
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02781
Reference40 articles.
1. Benzimidazolones: A New Class of Selective Peroxisome Proliferator-Activated Receptor γ (PPARγ) Modulators
2. Structural elucidation of rabeprazole sodium photodegradation products
3. Novel 1,3-dihydro-benzimidazol-2-ones and their analogues as potent non-nucleoside HIV-1 reverse transcriptase inhibitors
4. Synthesis of J-113397, the first potent and selective ORL1 antagonist
5. A Facile Route of Synthesis for Making Flibanserin
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