Dynamic Kinetic Asymmetric Transformations of Conduritol B Tetracarboxylates: An Asymmetric Synthesis of d-myo-Inositol 1,4,5-Trisphosphate
- 1 November 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 121 (46) , 10834-10835
- https://doi.org/10.1021/ja992960v
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- Dispiroketals in synthesis. Part 23.1 A new route to (+)-D-conduritol B from myo-inositolJournal of the Chemical Society, Perkin Transactions 1, 1997
- Asymmetric Total Synthesis of (+)-PancratistatinJournal of the American Chemical Society, 1995
- Chemical and enzymatic synthesis of glycoconjugates 1. Enzymatic galactosylation of conduritol BTetrahedron Letters, 1995
- Highly diastereoselective bis-hydroxylation of the amino-deoxy-conduritol C ring system. A formal synthesis of the aminocyclitol moiety of the antibiotic Hygromycin ATetrahedron Letters, 1995
- A synthetic route to valienamine: An interesting observation concerning stereoelectronic preferences in the SN2′ reactionTetrahedron Letters, 1994
- Synthesis of Optically Active 2,3,6-Tri-O-benzyl-D-myo-inositol from D-GlucoseChemistry Letters, 1991
- Total synthesis of antibiotic hygromycin AThe Journal of Organic Chemistry, 1991
- Synthesis of Optically Active Inositol Derivatives Starting from d-Glucurono-6,3-lactoneChemistry Letters, 1987
- Improved synthesis of conduritol B epoxideCarbohydrate Research, 1985
- The use of inhibitors in the study of glycosidasesBiochimie, 1982