Conformational Studies by Dynamic NMR. 90.1 Structure and Stereodynamics of the Rotamers of Di- and Tri-α-naphthylphenyl Derivatives
Author:
Affiliation:
1. Department of Organic Chemistry “A. Mangini”, University of Bologna, Viale Risorgimento, 4, Bologna 40136, Italy
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0258195
Reference14 articles.
1. Conformational Studies by Dynamic NMR. 89.1 Stereomutation and Cryogenic Enantioseparation of Conformational Antipodes of Hindered Aryl Oximes
2. Stable cis and trans rotational isomers of 1,8-di-o-tolylnaphthalene
3. Conformational Studies by Dynamic NMR. 86.1 Structure, Stereodynamics, and Cryogenic Enantioseparation of the Stereolabile Isomers of o-Dinaphthylphenyl Derivatives
4. Polar/.pi. interactions between stacked aryls in 1,8-diarylnaphthalenes
5. Synthesis and stereochemistry of novel triarylmesitylenes. Bases for rigid tridentate ligands
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