Microbial oxidation in synthesis: Preparation of 6-deoxy cyclitol analogues of myo-inositol 1,4,5-trisphosphate from benzene
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (27) , 3557-3560
- https://doi.org/10.1016/s0040-4039(00)99439-5
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- An efficient synthesis of optically active --inositol 1,4,5-triphosphateTetrahedron Letters, 1989
- Microbial oxidation in synthesis: Preparation from benzene of the cellular secondary messenger myo-inositol-1,4,5-trisphosphate (IP3) and related derivativesTetrahedron Letters, 1988
- A novel reagent for the synthesis of -inositol phosphates: ,-diisopropyl dibenzyl phosphoramiditeTetrahedron Letters, 1988
- Synthesis of inositol phosphatesJournal of the American Chemical Society, 1988
- Synthesis of DL--inositol 1,4,5-triphosphateTetrahedron Letters, 1987
- Microbial oxidation in synthesis: A six step perparation of (+)-pinitol from benzeneTetrahedron 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
- The allyl group for protection in carbohydrate chemistry. Part 18. Allyl and benzyl ethers of myo-inositol. Intermediates for the synthesis of myo-inositol trisphosphatesJournal of the Chemical Society, Perkin Transactions 1, 1987
- Total synthesis of optically active myo-inositol 1,4,5-tris(phosphate)Tetrahedron Letters, 1986