Concerning the Phosphorylation of Vicinal Diols
- 1 April 1988
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 18 (5) , 465-468
- https://doi.org/10.1080/00397918808060737
Abstract
The specific use of n-butyllithium as the base for reaction of diethyl phosphorochloridate with diols leads to the formation of diphosphate esters in good to excellent yields without any evidence for the formation of 5-, 6-, or 7-membered cyclic phosphates.Keywords
This publication has 12 references indexed in Scilit:
- Synthesis of DL--inositol 1,4,5-triphosphateTetrahedron Letters, 1987
- The total synthesis of D- and L-myo-inositol 1,4,5-trisphosphateJournal of the American Chemical Society, 1987
- Synthesis of -myo-inositol 1,4,5-triphosphateTetrahedron Letters, 1987
- Synthesis of myo-inositol 1-phosphate and 4-phosphate, and of their individual enantiomersJournal of the Chemical Society, Chemical Communications, 1987
- Bisphosphorylation of a vic-diol using a phosphite approach: synthesis of myo-inositol 4,5-bisphosphateJournal of the Chemical Society, Chemical Communications, 1987
- Total synthesis of optically active myo-inositol 1,4,5-tris(phosphate)Tetrahedron Letters, 1986
- Relative Reactivities of Hydroxyl Groups in CarbohydratesPublished by Elsevier ,1976
- 805. Cyclitols. Part X. Myoinositol phosphatesJournal of the Chemical Society, 1961
- Studies on myo-Inositol Phosphates of Natural OriginJournal of the American Chemical Society, 1959
- Cyclic Phosphates. III. Some General Observations on the Formation and Properties of Five-, Six- and Seven-membered Cyclic Phosphate EstersJournal of the American Chemical Society, 1957