Facial selectivity in addition reactions to the highly strained enone in tricyclo[5.2.1.02,6]deca-2(6),8-dienone and tricyclo[5.2.1.02,6]dec-2(6)-enone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Formal Synthesis of (±)-Aplykurodinone-1 through a Hetero-Pauson–Khand Cycloaddition Approach;Organic Letters;2017-02-20
2. Facial Selectivity in the Addition of Lithium Dimethylcuprate to 6-Substituted Tricyclo[5.2.1.02,6]deca-4,8-dienones. Synthesis of β-Substituted Cyclopentenones Using Flash Vacuum Thermolysis;Australian Journal of Chemistry;2014
3. Use of Flash Vacuum Thermolysis in a Stereocontrolled Synthesis of Optically Active Alkyl-substituted Cyclopentenones with Fragrant Properties;Australian Journal of Chemistry;2014
4. Beyond Frontier Molecular Orbital Theory: A Systematic Electron Transfer Model (ETM) for Polar Bimolecular Organic Reactions;The Journal of Organic Chemistry;2012-11-02
5. Addition Reactions: Polar Addition;Organic Reaction Mechanisms Series;2011-12-06
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