The reversion reactions of d-glucose during the hydrolysis of cellulose with dilute sulfuric acid
β Scribed by Richard F. Helm; Raymond A. Young; Anthony H. Conner
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 865 KB
- Volume
- 185
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
In the hydrolysis of O-(2-hydroxypropyl)cellulose, residues of D-gh.ICOSe substituted with a single O-(2-hydroxypropyl) substituent at O-2 (irrespective of the pattern of additional substitution at O-3 or O-6) form 1,2-0-(1-methyl-1,2ethanediyl)-a-D-glucose acetals. Based on the characteristics of 2
The syntheses of the styryl lactones (+)-goniofufurone ( ) and (+)-7-epi-goniofufurone (2) from Dglucose are presented. The key steps are the formation of the lactone moiety by reaction of the hemiace~ais 15 and 16 with meldrum's acid (3) and the addition of phenylmagnesium bromide to the aldehydes
Application of the Reaction of D-