ge~~~~tha~~~mdl~t~i~~ofa~lortho-~~~rl~~~ofa~,tha~tnrctunof~ohhu~~~of 2,3:5,64i4-~o~ro~yudene~-amrmi~1 w M through the w l tcm~tC-luKlC-4to~aarLwldc4l. 10 have reported (1) Wt bir(l,24-ieopmpylidene-34-thhaWmyl-Q-p-e-furamae)dWAfldeundergoeea w-fragmentawon ~tunug hpyrpJrridha to give equh01u? mtd 0f
IMPROVED PREPARATION OF DI-O-ISOPROPYLIDENE-1,2;5,6-D-MANNITOL
β Scribed by Morpain, C.; Nasser, B.; Laude, B.; Latruffe, N.
- Book ID
- 120056551
- Publisher
- Taylor and Francis Group
- Year
- 1990
- Tongue
- English
- Weight
- 251 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0030-4948
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Three different methods of acetonation of D-mannitol using (a) acetone and zinc chloride, (6), 2,2\_dimethoxypropane, l,Zdimethoxyethane, and tin(I1) chloride, and (c) 2-methoxypropene, N, N-dimethylformamide, and p-toluenesulfonic acid were studied in detail and compared, using gas-liquid chromatog
1,2:5,6-Di-0-isopropylidene-o-mannitol (1) is the most important source of o-glyceraldehyde derivatives which are usedIe widely in synthesis. The formation of 1 from o-mannitol (2) has been studied severally"5. All of the syntheses require the separation of 1 from the accompanying 1,2:3,4:5,6\_tria