Face selectivity in the reactions of 2,4-disubstituted adamantanes and their modification by inclusion in β-cyclodextrin solutions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference52 articles.
1. Face Selection in Addition and Elimination in Sterically Unbiased Systems
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3. Orbital-Controlled Stereoselections in Sterically Unbiased Cyclic Systems
4. Origin of Facial Diastereoselection. Evidence for Negative Role of Antiperiplanar Hyperconjugation Effects in the Transition State of Carbene Insertion
5. Reversal of Diastereoselectivities in Intra- and Intermolecular Reactions of 2-Adamantanylidenes Primarily Caused by Electron-Donating and Electron- Withdrawing Substituents on C5
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1. Orbital Phase Environments and Stereoselectivities;Orbitals in Chemistry;2009
2. 1,3-Dithioles;Comprehensive Heterocyclic Chemistry III;2008
3. A novel photoinduced ring opening and isomerization of adamantane-2-spiro isoxazolines using Mo(CO)6;Tetrahedron Letters;2006-10
4. Regioselectivity in the 1,3-dipolar cycloaddition of adamantylidenefulvene and its modification by inclusion in cyclodextrins' solutions;Tetrahedron;2006-07
5. Synthetic Studies on Allelopathic Terpenoids;Journal of Synthetic Organic Chemistry, Japan;2006
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