Organophosphorus Chemistry. 2. The Reduction of Quinquevalent Phosphrous to the Trivalent State
- 1 May 1988
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 18 (7) , 665-670
- https://doi.org/10.1080/00397918808077352
Abstract
Phosphoryl and phosphonyl chlorides are reduced conveniently to the monobasic acid forms of the corresponding phosphorous and phosphonous acids by the use of sodium borohydride dispersed in dioxane.Keywords
This publication has 8 references indexed in Scilit:
- Synthesis of Carbon-Phosphorus BondsPublished by Taylor & Francis ,2003
- A Mechanistic Investigation of the Todd ReactionBulletin of the Chemical Society of Japan, 1985
- Convenient procedure for the synthesis of phosphorus-carbon bonds using sodium bis(2-methoxyethoxy)aluminum hydrideJournal of the American Chemical Society, 1972
- Stereospecific alkylation of menthyl phenylphosphinateJournal of the American Chemical Society, 1970
- Stereospecific synthesis and reactions of optically active isopropyl methylphosphinateJournal of the American Chemical Society, 1970
- Reduktion organischer Verbindungen des fünfwertigen Phosphors zu Phosphinen, II. Reduktion tertiärer Phosphinoxyde zu tertiären Phosphinen mit TrichlorsilanEuropean Journal of Inorganic Chemistry, 1965
- Characteristic infrared absorption frequencies of organophosphorus compounds—I The phosphoryl (PO) groupSpectrochimica Acta, 1964
- Phosphororganische Verbindungen, XVI. Wege zur Darstellung primärer, sekundärer und tertiärer PhosphineEuropean Journal of Inorganic Chemistry, 1958