𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of protected myo-inositols

✍ Scribed by Ian H. Gilbert; Andrew B. Holmes; Rodney C. Young

Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
133 KB
Volume
31
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Synthesis of some myo-inositol nitrates
Synthesis of some myo-inositol nitrates
✍ Mario Brufani; Maria C. Cesta; Lucia Donnarumma; Luigi Filocamo; Gianluca Gostol πŸ“‚ Article πŸ“… 1991 πŸ› Elsevier Science 🌐 English βš– 252 KB
Synthesis of some carbamates of myo-inos
Synthesis of some carbamates of myo-inositol
✍ Mario Brufani; Maria C. Cesta; Lucia Donnarumma; Luigi Filocamo; Gianluca Gostol πŸ“‚ Article πŸ“… 1992 πŸ› Elsevier Science 🌐 English βš– 453 KB

The syntheses are described of the 1-O-carbamoyl (11), 1-O-carbamoyl-2-O-stearoyl (10), 1-O-(acetylcarbamoyl)-2-O-stearoyl (12), 1-O-(heptylcarbamoyl) (13), 2-O-(heptylcarbamoyl) (14) 1,2-di-O-(heptylcarbamoyl) (15), and 1-O-(octadecylcarbamoyl) (16) derivatives of myo-inositol. None of these compou

Synthesis of the enantiomeric 1,4,5,6-te
Synthesis of the enantiomeric 1,4,5,6-tetra-O-benzyl-myo inositols
✍ Karol S. Bruzik; Grzegorz M. SalamoΕ„czyk πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 English βš– 490 KB

The synthesis of the optically pure 1,4,5,6-tetra-O-benzyl-myo-inositols was achieved in four steps via diastereomeric 2,3-spire-acetals of myo-inositol with Land D-camphor as the key intermediates. Camphor dimethyl acetal was used for the acetalation reaction. The diastereomers were benzylated and