Stereoelectronic Effects on the One-Electron Donor Reactivity of Trivalent Phosphorus Compounds. Experimental and Theoretical Investigations
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/71/4/71_4_927/_pdf
Reference26 articles.
1. Dichotomy in the Reactivity of Trivalent Phosphorus Compounds Z 3 P (Z = Ph, n Bu, OR) Observed in the Photoreaction with a Ruthenium Complex
2. Dediazoniation of arenediazonium salts with trivalent-phosphorus compounds. Tool for examination of the reactivity of phosphorus-centered radicals
3. Reactivity of Phosphorus-Centered Radicals Generated during the Photoreaction of Diphenylphosphinous Acid with 10-Methylacridinium Salt
4. Reaction of a cation radical generated from trivalent phosphorus compound through single-electron transfer to arenediazonium salt
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1. Irreversibility of Single Electron Transfer Occurring from Trivalent Phosphorus Compounds to Iron(III) Complexes in the Presence of Ethanol;Bulletin of the Chemical Society of Japan;2002-06
2. Kinetic study on debromination ofvic-dibromides with trivalent phosphorus compounds;Heteroatom Chemistry;2001
3. Quenching of a Photosensitized Dye through Single-Electron Transfer from Trivalent Phosphorus Compounds;The Journal of Organic Chemistry;2000-06-29
4. Reactivity of a trivalent phosphorus radical cation as an electrophile toward pyridine derivatives;Heteroatom Chemistry;2000
5. Fluorescence Quenching of Rhodamine Through Single-Electron Transfer from Trivalent Phosphorus Compounds;Phosphorus, Sulfur, and Silicon and the Related Elements;1999-01-01
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