Spectroscopic Evidences for the Hyperconjugative Interaction in 2-Bromosubstituted Acetophenones
Author:
Publisher
Informa UK Limited
Subject
Spectroscopy,Atomic and Molecular Physics, and Optics,Analytical Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00387018908053927
Reference17 articles.
1. Conformational studies of α-substituted carbonyl compounds. Part 1. Conformation and electronic interaction in hetero-substituted acetones by infrared and ultraviolet spectroscopy
2. Electronic interaction in heterosubstituted acetones studied by means of ultraviolet photoelectron and electron transmission spectroscopy
3. Conformational studies of α-substituted carbonyl compounds—V. Evidence for hyperconjugative interactions in 2-iodosubstituted carbonyl systems. ω-iodo-p-substituted acetophenones
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1. Conformational preferences of α-fluoroketones may influence their reactivity;Beilstein Journal of Organic Chemistry;2017-12-29
2. Conformational and electronic interaction studies of some p-substituted α-bromo-α-ethylsulfonylacetophenones;Journal of Molecular Structure: THEOCHEM;2004-02
3. CONFORMATIONAL AND ELECTRONIC INTERACTION STUDIES OF α-SUBSTITUTED CARBONYL COMPOUNDS. XI. ω-(p-PHENYLTHIO)-p-SUBSTITUTED ACETOPHENONES;Phosphorus, Sulfur, and Silicon and the Related Elements;1992-03
4. Conformational and electronic interaction studies of α-substituted carbonyl compounds. Part 9. ω-Hetero-substituted acetophenones;J. Chem. Soc., Perkin Trans. 2;1990
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