Stable Simple Enols. Resolution of Chiral 1-[9‘-(2‘-Fluoroanthryl)]-2,2-Dimesitylethenol. A Different Racemization Mechanism for the Enol and its Acetate1
Author:
Affiliation:
1. Department of Organic Chemistry, The Hebrew University, Jerusalem 91904, Israel
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo020497q
Reference27 articles.
1. Presented in part in the 13thIUPAC Conference on Physical Organic Chemistry, Seoul, Korea, August 25−29, 1996; Rappoport, Z.; Frey, Y.; Sigalov, M.; Rochlin, E.Pure Appl. Chem.1997,69, 1933.
2. Threshold Rotational Mechanisms and Enantiomerization Barriers of Polyarylvinyl Propellers
3. Stable simple enols. 3. Static and dynamic NMR behavior of crowded triarylethenols and related compounds. Three-ring flip as the threshold mechanism for enantiomerization of crowded triarylvinyl propellers
4. Fluorine Magnetic Resonance Studies of Conformational Interconversion Rates in Triphenylcarbonium Ions
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