Synthesis and degenerate cope rearrangement of 2,6-diphenylbarbaralane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference152 articles.
1. The degenerate Cope Rearrangement in 2,6‐Barbaralanedicarbonitrile
2. The Role of Neighboring Groups in Replacement Reactions. XIV. The 5,6-Double Bond in Cholesteryl p-Toluenesulfonate as a Neighboring Group
3. Small-Ring Compounds. XV. Methylenecyclobutene and Related Substances1
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1. Syntheses and Structures of 2,6-Substituted Barbaralanes;Liebigs Annalen;2006-01-25
2. The Search for Bishomoaromatic Semibullvalenes and Barbaralanes: Computational Evidence of Their Identification by UV/Vis and IR Spectroscopy and Prediction of the Existence of a Blue Bishomoaromatic Semibullvalene;Journal of the American Chemical Society;2002-03-07
3. Lifting of the Degeneracy in Semibullvalenes by Remote and Direct Substituents: A Quantitative Study Using Variable-Temperature Carbon-13 NMR Spectroscopy;The Journal of Organic Chemistry;2001-02-20
4. Perturbation of Degeneracy of the Cope Rearrangement by the Crystal Lattice of the β-Form of 1,5-Dimethylsemibullvalene-2,6-dicarbonitrile As Studied by Variable-Temperature Solid-State Carbon-13 Spectroscopy and X-ray Crystallography at Cryogenic Temperatures;Journal of the American Chemical Society;2000-04-25
5. Extension of Saunders' Isotopic Perturbation Method as Probe for the Structures in Solution of 2,4,6,8-Substituted Barbaralanes – NMR-Spectroscopic Evidence for the Coexistence of Localised and Delocalised States[1];European Journal of Organic Chemistry;1999-11
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