The Conformations of Several 1-Phenylethyl and 1-Phenylpropyl Aryl Sulfoxides. Evidence for Attractive Aryl/Aryl Interaction
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/55/11/55_11_3560/_pdf
Reference21 articles.
1. The Conformations of 2-Phenylpropionaldehyde and Some Aliphatic Ketones. The Possible Importance of the CH/π and CH/n Interactions in Determining the Molecular Geometry of a Mobile System
2. Novel route to racemization of sulfoxides
3. Oxygen-17 Nuclear Magnetic Resonance. III. Oxygen Atoms with a Coordination Number of Two
4. The Conformations of Several Aliphatic Alcohols. The General Occurrence of the Attractive Alkyl/Phenyl Interaction
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3. Enantioselective Photooxidation of a Sulfide by a Chiral Ruthenium(II) Complex Immobilized on a Montmorillonite Clay Surface: The Role of Weak Interactions in Asymmetric Induction;The Journal of Physical Chemistry B;2006-01-24
4. The Conformation of 2-Phenylpropionaldehyde and Alkyl 1-Phenylethyl Ketones as Evidenced by Ab Initio Calculations. Relevance of the CH/π and CH/O Interactions in Stereochemistry;Bulletin of the Chemical Society of Japan;2002-08
5. From Sulfoxide Precursors to Model Oligomers of Conducting Polymers;Journal of the American Chemical Society;2002-05-31
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