A Stereodynamic Probe Providing a Chiroptical Response to Substrate-Controlled Induction of an Axially Chiral Arylacetylene Framework
Author:
Affiliation:
1. Department of Chemistry, Georgetown University, Washington, D.C. 20057, United States
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja111583e
Reference101 articles.
1. Stereochemistry of Biphenyls. LI. Resolution of Diphenic Acids Having Many-Membered Bridges Across the 5,5'-Positions: A Novel Type of Restricted Rotation1
2. The Calculation and Determination of the Buttressing Effect for the Racemization of 2,2',3,3'-Tetraiodo-5,5'-dicarboxybiphenyl
3. 101. Some racemisation data for compounds owing their optical activity to restricted rotation
4. Stereochemistry of the 1,2,3,4-Dibenzcyclonona-1,3-diene System.1 A Note on the Racemization Barrier in Bridged Biphenyls
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