Using Computational Chemistry to Rationalize the Diastereoselectivity of the Borohydride Reduction of Benzoin
Author:
Affiliation:
1. Department of Chemistry, University of Wisconsin−Madison, 1101 University Avenue, Madison, Wisconsin 53706, United States
Publisher
American Chemical Society (ACS)
Subject
Education,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jchemed.2c00828
Reference26 articles.
1. The determination of the stereochemistry of erythro-1,2-diphenyl-1,2-ethanediol: an undergraduate organic experiment
2. Diastereoselectivity in the Reduction of α-Hydroxyketones. An Experiment for the Chemistry Major Organic Laboratory
3. Mohrig, J. R.; Hammond, C. N.; Schatz, P. F.; Morrill, T. C. In Modern Projects and Experiments in Organic Chemistry: Miniscale and Williamson Microscale, 2nd ed. Macmillan, 2003; pp 363–373.
4. Using NMR Spectroscopy To Probe the Chemo- and Diastereoselectivity in the NaBH4 Reduction of Benzoin Acetate and Benzoin Benzoate
5. Using NMR Spectroscopy and Chemical Synthesis to Establish Diastereoselectivity of NaBH4 and Meerwein–Ponndorf–Verley (MPV) Reduction of (±)-Benzoin Isopropyl Ether: A Collaborative Discovery-Based Laboratory Experiment
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1. Integrating Computational Chemistry into Secondary School Lessons;Journal of Chemical Education;2024-05-21
2. Highly Reversed Diastereoselective Meerwein–Ponndorf–Verley (MPV) Reductions of Benzoin and Benzoin Pivalate Leading to meso- and dl-Hydrobenzoins: A Collaborative Stereochemical Investigation Using NMR Spectroscopy and Chemical Synthesis;Journal of Chemical Education;2023-12-29
3. A Computational Chemistry Course for Teachers: From Research Laboratories to High-School Chemistry Teaching;Journal of Chemical Education;2023-10-26
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