Chemo-/regio-selective synthesis of 2-aryl-3-acetyl-2,4-dihydro-1H-5H-1,5-benzodiazepines using Lewis acid, CeCl3·7H2O
Author:
Funder
National Natural Science Foundation of China
Natural Science Foundation of Hebei Province
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference42 articles.
1. Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists
2. Preyssler catalyst-promoted rapid, clean, and efficient condensation reactions for 3H-1,5-benzodiazepine synthesis in solvent-free conditions
3. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures
4. Electroactive 1,5-benzodiazepines bearing either a tetrathiafulvalene or a ferrocene moiety
5. Facile synthesis of both perfluoroalkyl and phosphonate groups substituted trans-1,5-benzodiazepine and its derivatives via a one-pot catalyst-free process
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