TiCl4 promoted three component coupling reaction: an efficient method for the substituted tetrahydropyrilidene acetates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Synthetic routes to 2,5-disubstituted tetrahydrofurans
2. The Addition Reaction of Acetals to Activated Olefins under Extremely Mild Conditions
3. TiCl4 promoted three component coupling reaction: A new method for the synthesis of functionalized tetrahydrofurans and tetrahydropyrans
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1. TiCl4-Promoted Tandem Carbonyl or Imine Addition and Friedel–Crafts Cyclization: Synthesis of Benzo-Fused Oxabicyclooctanes and Nonanes;Organic Letters;2012-04-04
2. Synthesis of γ-amino alcohols from aldehydes, enamines, and trichlorosilane using Lewis base catalysts;Tetrahedron;2011-01
3. Capturing the Essence of Organic Synthesis: From Bioactive Natural Products to Designed Molecules in Today’s Medicine;The Journal of Organic Chemistry;2010-10-11
4. Influence of the Reaction Conditions on the Evolution of the Michael Addition of β-Keto Sulfones to α,β-Unsaturated Aldehydes;European Journal of Organic Chemistry;2010-06-25
5. ChemInform Abstract: TiCl4-Promoted Three-Component Coupling Reaction: An Efficient Method for the Substituted Tetrahydropyrilidene Acetates.;ChemInform;2010-06-13
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