Leaving-group effects and ion-pair intermediates in base-promoted elimination competing with base-catalyzed 1,3-proton transfer
Author:
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja00466a028
Cited by 61 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
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2. Does Activation of the Anti Proton, Rather than Concertedness, Determine the Stereochemistry of Base-Catalyzed 1,2-Elimination Reactions? Anti Stereospecificity in E1cB Eliminations of β-3-Trifluoromethylphenoxy Esters, Thioesters, and Ketones;The Journal of Organic Chemistry;2012-02-24
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4. Evidence of a Borderline Region between E1cb and E2 Elimination Reaction Mechanisms: A Combined Experimental and Theoretical Study of Systems Activated by the Pyridine Ring;Journal of the American Chemical Society;2005-10-11
5. Solvent Free Vapor Phase Photografting of Maleic Anhydride onto Poly(ethylene terephthalate) and Surface Coupling of Fluorinated Probes, PEG, and an RGD-Peptide;Biomacromolecules;2005-06-02
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