Rapid Access to Tricyclic Systems: Highly Endoselective Diels-Alder Reaction of Cycloalkenones with Cyclic Dienes Under Microwave Irradiation
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1081/SCC-120026847
Reference9 articles.
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3. Diels-Alder reactions of cycloalkenones. 16. The Endo diastereoselectivity of some cycloalkenones in reactions with 1,3-cyclohexadiene
4. APPLICATIONS OF MICROWAVE ENERGY IN ORGANIC CHEMISTRY. A REVIEW
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2. Achieving Enantioselectivity in Difficult Cyclohexa-1,3-diene Diels–Alder Reactions with Sulfur-Stabilized Silicon Cations as Lewis Acid Catalysts;Organic Letters;2018-10-26
3. Refinement of the Catalyst Backbone of Chiral Intramolecular Silicon-Sulfur Lewis Pairs: Improved Enantioselectivity in the Diels-Alder Reaction of Cyclohexa-1,3-diene and Chalcone Derivatives;European Journal of Organic Chemistry;2018-05-03
4. Enantioselective Diels–Alder Reactions of Cyclohexa-1,3-diene and Chalcones Catalyzed by Intramolecular Silicon–Sulfur Lewis Pairs as Chiral Lewis Acids;Organometallics;2016-08-12
5. DFT study on the mechanism of the Diels–Alder reactions leading to bicyclo[4.2.0]octenones;Progress in Reaction Kinetics and Mechanism;2016-03
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