Stereoselection of sterically unbiased Diels–Alder dienes with spiro conjugation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
1. Orbital-Controlled Stereoselections in Sterically Unbiased Cyclic Systems
2. Stereoelectronic Control in Diels−Alder Reaction of Dissymmetric 1,3-Dienes
3. Stereochemistry of nucleophilic addition to cyclohexanone. The importance of two-electron stabilizing interactions
4. Heteroatom-directed .pi.-facial diastereoselection in Diels-Alder cycloadditions of plane-nonsymmetric cyclopentadienes
5. The “cieplak effect”: Hyperconjugative interactions in diels alder reactions.
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1. ON/OFF Spiroconjugation through Peripheral Functionalization: Impact on the Reactivity and Chiroptical Properties of Spirobifluorenes;ChemPlusChem;2022-04-12
2. Probing the role of solvation in predicting the π-facial selectivity of 5-Fluoro-2-methyleneadamantane with per-acid: A case study;Computational and Theoretical Chemistry;2013-12
3. A computational approach towards predicting π-facial selectivity in sterically unbiased olefins: an evaluation of the relative importance of electrostatic and orbital effects;Tetrahedron;2011-05
4. Orbital Phase Environments and Stereoselectivities;Orbitals in Chemistry;2009
5. Contrasteric Diels–Alder reactions of 5-methyl-5-phenylcyclopentadiene;Tetrahedron Letters;2008-03
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