𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Stereoselective Synthesis of myo-Inositol-1,3,4,5-tetrakisphosphate Analogues from 6-Deoxy D-Inositol Precursors.

✍ Scribed by Didier Dubreuil; Jeannine Cleophax; Mauro Vieira de Almeida; C. Verre-Sebrie; Muriel Pipelier; Georges Vass; Stephane D. Gero

Publisher
John Wiley and Sons
Year
2010
Weight
25 KB
Volume
30
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Synthesis of the Enantiomers of 6-Deoxy-
Synthesis of the Enantiomers of 6-Deoxy-myo-Inositol 1,3,4,5-Tetrakisphosphate, Structural Analogues of myo-Inositol 1,3,4,5-Tetrakisphosphate
✍ Graeme Horne; Barry V. L. Potter πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 25 KB

In the paper by G. Horne and B. V. L. Potter published in Chem. Eur. J. 2001, 7, 80, there is a mistake in the drawing of some regiochemistry of the structural diagrams in Schemes 1 Β± 3. The correct structures are given below.

ChemInform Abstract: Stereoselective Syn
ChemInform Abstract: Stereoselective Synthesis of 6-Deoxy and 3,6-Dideoxy-D-myo-inositol Precursors of Deoxy-myo-inositol Phosphate Analogues from D-Galactose.
✍ D. DUBREUIL; J. CLEOPHAX; M. VIEIRA DE ALMEIDA; C. VERRE-SEBRIE; J. LIAIGRE; G. πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 41 KB πŸ‘ 1 views

Stereoselective Synthesis of 6-Deoxy and 3,6-Dideoxy-D-myo-inositol Precursors of Deoxy-myo-inositol Phosphate Analogues from D-Galactose. -The key step in the synthesis of the title compounds is the Ferrier rearrangement of pyranoside (II). Both resulting cyclohexanones (III) and (IV) can be trans