Easy access of optically active myo-inositol derivatives by enantioselective acylation using a tartaric acid monoester
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (18) , 2613-2616
- https://doi.org/10.1016/0040-4039(90)80139-d
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Total syntheses of chiral sn-myo-inositol-1,4,5-trisphosphate1 and its enantiomerTetrahedron Letters, 1989
- Metabolism of the inositol phosphates produced upon receptor activationBiochemical Journal, 1989
- Recent developments in the synthesis of myo-inositol phosphatesChemical Society Reviews, 1989
- A Synthesis of 1D‐ and 1L‐myo‐Inositol 1,3,4,5,‐TetraphosphateHelvetica Chimica Acta, 1988
- Synthesis of Optically Active myo-Inositol 1,3,4-TrisphosphateChemistry Letters, 1988
- The total synthesis of D- and L-myo-inositol 1,4,5-trisphosphateJournal of the American Chemical Society, 1987
- The metabolism and function of inositol phosphatesBiochemical Society Transactions, 1987
- Synthesis of Optically Active Inositol Derivatives Starting from d-Glucurono-6,3-lactoneChemistry Letters, 1987
- Synthesis of myo-inositol 1-phosphate and 4-phosphate, and of their individual enantiomersJournal of the Chemical Society, Chemical Communications, 1987
- Total synthesis of optically active myo-inositol 1,4,5-tris(phosphate)Tetrahedron Letters, 1986