Mild synthesis of enantiomerically pure imidazo-[1,2- a ]azepines mediated by Yb(OTf) 3
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Analogs of 3-Hydroxy-1H-1-benzazepine-2,5-dione: Structure−Activity Relationship at N-Methyl-d-aspartate Receptor Glycine Sites
2. d-Fused [1]Benzazepines with Selective in Vitro Antitumor Activity: Synthesis and Structure−Activity Relationships
3. Diastereoselective synthesis of 1,2-diphenyl-1,2-diaminoethanes by Yb(OTf)3 accelerated reductive coupling of imines
4. Multiple diamine-dialdehyde condensations. Synthesis of heterocyclic dodecalenes
5. Regioselective diamine-dialdehyde condensation. Annelated azepinopurine
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1. Synthesis of Axially Chiral Biaryls via Enantioselective Ullmann Coupling of ortho ‐Chlorinated Aryl Aldehydes Enabled by a Chiral 2,2′‐Bipyridine Ligand;Angewandte Chemie International Edition;2022-10-21
2. Synthesis of Axially Chiral Biaryls via Enantioselective Ullmann Coupling of ortho ‐Chlorinated Aryl Aldehydes Enabled by a Chiral 2,2′‐Bipyridine Ligand;Angewandte Chemie;2022-10-21
3. Ytterbium Triflate Catalyzed Synthesis of Heterocycles;Synthesis;2016-12-01
4. ChemInform Abstract: Mild Synthesis of Enantiomerically Pure Imidazo-[1,2-a]azepines Mediated by Yb(OTf)3.;ChemInform;2010-05-21
5. Nickel-Catalyzed Asymmetric Ullmann Coupling for the Synthesis of Axially Chiral Tetra-ortho-Substituted Biaryl Dials;Organic Letters;2010-01-29
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