Electronic structure and reactivity of propellanes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference36 articles.
1. Propellanes as stereochemical models
2. Propellanes. XLVI. Steric and electronic effects as observed in reactions of propellanes
3. Reaction of bicyclic dienes with 4-substituted-1,2,4-triazoline-3,5-diones
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1. Orbital Phase Environments and Stereoselectivities;Orbitals in Chemistry;2009
2. Stereoselectivity Control by Oxaspiro Rings during Diels−Alder Cycloadditions to Cross-Conjugated Cyclohexadienones: The Syn Oxygen Phenomenon;Journal of the American Chemical Society;2004-12-01
3. Stereoselection of sterically unbiased Diels–Alder dienes with spiro conjugation;Tetrahedron Letters;2001-07
4. Role of Heteroatoms in Diastereofacial Control in Cycloaddition to a Dissymmetric Cyclohexa-1,3-diene Moiety in a Polycyclic Framework. Remarkable Stereodirecting Influence of Distal Protective Groups;The Journal of Organic Chemistry;2000-02-24
5. Stereoelectronic Control in Diels−Alder Reaction of Dissymmetric 1,3-Dienes;Accounts of Chemical Research;2000-02-11
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