Use of 1H, 13C, and 19F-NMR Spectroscopy and Computational Modeling To Explore Chemoselectivity in the Formation of a Grignard Reagent
Author:
Affiliation:
1. Department of Chemistry, Winona State University, Winona, Minnesota 55987, United States
2. Department of Chemistry, University of Wisconsin−Madison, Madison, Wisconsin 53706, United States
Publisher
American Chemical Society (ACS)
Subject
Education,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ed500700c
Reference16 articles.
1. A serendipitous two-step synthesis from a Grignard reaction: 1-ethoxy-1,1,1-triphenlymethane from the reaction of phenylmagnesium bromide with benzophenone
2. Grignard Reaction of an Epoxide: A Mechanistic Study
3. Diastereoselective Synthesis of (+/-)-1,2-Diphenyl-1,2-propanediol. A Discovery-Based Grignard Reaction Suitable for a Large Organic Lab Course
4. Using a Premade Grignard Reagent To Synthesize Tertiary Alcohols in a Convenient Investigative Organic Laboratory Experiment
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