Desymmetrization of myo-inositol
| Title | Desymmetrization of myo-inositol |
| Publication Type | Journal Article |
| Year of Publication | 2025 |
| Authors | Patil, NT, Patil, MT, Gonnade, RG, Shashidhar, MS |
| Journal | Carbohydrate Research |
| Volume | 553 |
| Pagination | 109505 |
| Date Published | JUL |
| Type of Article | Article |
| ISSN | 0008-6215 |
| Keywords | Conglomerate, Crystallization, Cyclitol, Enantiomers, Inositol, Lipid |
| Abstract | Chemistry and biology of phosphoinositols have been intensely investigated areas of research over the last 4-5 decades due to their involvement in cellular signal transduction pathways. Efficient laboratory synthesis of enantiomeric derivatives of inositols was a central issue since they were required for the delineation of the myo-inositol cycle as well as for the total synthesis of polyol based natural products and their derivatives. This essentially meant the development of competent methods for the desymmetrization of myo-inositol leading to the preparation of enantiomeric O-substituted derivatives of myo-inositol. This was approached by: the classical resolution methods involving separable diastereomers, the chiral pool synthesis, enzyme catalysis, asymmetric catalysis and preferential crystallization of enantiomers in a racemic conglomerate. This review summarizes results obtained in author's laboratory, as well as those reported in the literature on attempts at desymmetrization of myo-inositol. |
| DOI | 10.1016/j.carres.2025.109505 |
| Type of Journal (Indian or Foreign) | Foreign |
| Impact Factor (IF) | 2.5 |
