Sequential Addition of Amines to Nitrile and Carbon–Carbon Multiple Bond: A Route to 7-Amino-5H-dibenzo[c,e]azepines
Author:
Affiliation:
1. Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200438, China
2. State Key Laboratory of Organometallic Chemistry, Shanghai 200032, China
Funder
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02540
Reference44 articles.
1. Hypolipidemic Activity of 6-Substituted 6, 7-Dihydro-5H-dibenz[c,e]azepine and the effects of 6, 7-dihydro-5H-dibenz[c,e]azepine on Lipid Metabolism of Rodents
2. Synthesis and biological evaluation of novel bifendate derivatives bearing 6,7-dihydro-dibenzo[c,e]azepine scaffold as potent P-glycoprotein inhibitors
3. Basic N-interlinked imipramines show apoptotic activity against malignant cells including Burkitt’s lymphoma
4. Identification of a Benzoisoxazoloazepine Inhibitor (CPI-0610) of the Bromodomain and Extra-Terminal (BET) Family as a Candidate for Human Clinical Trials
5. Efficient Organocatalytic Cross-Aldol Reaction between Aliphatic Aldehydes through Their Functional Differentiation
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