2,3:6,7-Di-O-diethylidene-d-glycero-l-talo-heptono-1,4-lactone
✍ Scribed by Håkansson, Anders E. ;van Ameijde, Jeroen ;Horne, Graeme ;Guglielmini, Luisa ;Nash, Robert J. ;Fleet, George W.J. ;Watkin, David J.
- Book ID
- 104487515
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 532 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
The title compound, C 15 H 17 N 3 O 5 , was formed by carrying out a Wittig reaction, under basic conditions, on 2-azido-3,5±Obenzylidene-2-deoxy-d-lyxose.
A second crystalline diacetonide, the title compound, C 13 H 20 O 7 , has been isolated from the sequential treatment of d-tagatose with aqueous sodium cyanide, followed by acetone in the presence of acid. Structural ambiguities with regard to the size of both the lactone and ketal rings are resolve