Substituent effects and additivity in the carbon-13 nuclear magnetic resonance spectra of chlorinated naphthalenes and their chlorinated naphthol metabolites
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00403a031
Cited by 44 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. Cu–Mn Spinel Oxide Catalyzed Regioselective Halogenation of Phenols and N-Heteroarenes;The Journal of Organic Chemistry;2012-06-15
2. Systematic discrepancy of theoretical predictions of NMR chemical shifts for chlorinated aromatic carbons using the GIAO DFT method;Molecular Physics;2004-09-20
3. Carbon−Carbon Bond-Forming Reductive Elimination from Arylpalladium Complexes Containing Functionalized Alkyl Groups. Influence of Ligand Steric and Electronic Properties on Structure, Stability, and Reactivity;Organometallics;2004-06-04
4. The Prediction of the13C NMR Signal Positions in Substituted Naphthalenes, Part 2: The Use of Statistical Substituent Chemical Shift (SSCS) Values;Spectroscopy Letters;2000-03
5. Prediction of 13 C NMR chemical shifts in substituted naphthalenes;Theoretical Chemistry Accounts: Theory, Computation, and Modeling (Theoretica Chimica Acta);1999-05-25
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