𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective synthesis of highly substituted 8-oxabicyclo[3.2.1]octanes and 2,7-dioxatricyclo[4.2.1.03,8]nonanes

✍ Scribed by Dmitry A. Khlevin; Sergey E. Sosonyuk; Marina V. Proskurnina; Nikolay S. Zefirov


Book ID
116909477
Publisher
Elsevier Science
Year
2012
Tongue
French
Weight
642 KB
Volume
68
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Synthesis of dioxatricyclic segments of
✍ J. Wittenberg; W. Beil; H.M.R. Hoffmann πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 237 KB

Starting from 1,1-bisbenzyloxy propanone four oxetanes A, B, C and D representing the dioxatricyclic core of dictyoxetane were synthesized. All of them show a cytotoxic/cytostatic effect using a human gastric carcinoma and a human heptocellular cell line. The activity is comparable to that of5-fluor

(Β±)-exo-2-HydrΒ­oxy-5-oxo-4,8-dioxatricyc
✍ Sadeghi-Khomami, Ali ;Thomas, Neil R. ;Wilson, Claire πŸ“‚ Article πŸ“… 2006 πŸ› International Union of Crystallography 🌐 English βš– 213 KB

The title compound, C 8 H 9 NO 5 , was prepared as a by-product in synthetic efforts to prepare a carbasugar analogue of a putative intermediate, viz. (AE)-6-hydroxymethyl-7-oxabicyclo[2.2.1]hept-2-exo-3-endo-diol, in the uridine diphosphate-galactopyranose mutase-catalysed reaction. The structure s