A serendipitous two-step synthesis from a Grignard reaction: 1-ethoxy-1,1,1-triphenlymethane from the reaction of phenylmagnesium bromide with benzophenone
Author:
Publisher
American Chemical Society (ACS)
Subject
Education,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ed069p76
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Use of 1H, 13C, and 19F-NMR Spectroscopy and Computational Modeling To Explore Chemoselectivity in the Formation of a Grignard Reagent;Journal of Chemical Education;2015-02-09
2. The Question-Driven Laboratory Exercise: A New Pedagogy Applied to a Green Modification of Grignard Reagent Formation and Reaction;Journal of Chemical Education;2010-05-13
3. Titanium(IV) complexes containing mono-cyclopentadienyl and bulky trityloxy mixed ligands: synthesis and polymerization activity;Applied Organometallic Chemistry;2005
4. Diastereoselective Synthesis of (+/-)-1,2-Diphenyl-1,2-propanediol. A Discovery-Based Grignard Reaction Suitable for a Large Organic Lab Course;Journal of Chemical Education;2001-04
5. Grignard Synthesis of Various Tertiary Alcohols;Journal of Chemical Education;1998-01
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