The biantennary oligosaccharide glycoside beta-D-GlcpNAc-(1----2)-alpha-D- Manp-(1----3)- [beta-D-GlcpNAc-(1----2)-alpha-D-Manp-(1----6)]-beta-D-Manp- OR is a potential substrate for N-acetylglucosaminyltransferases (GlcNAcTs) III-V. The dideoxypentasaccharide glycoside beta-D-GlcpNAc-(1----2)-4- de
Use of N-acetylglucosamiyltransferases I and II in the synthesis of a dideoxypentasaccharide
β Scribed by Gordon Alton; Geeta Srivastava; Kanwal J. Kaur; Ole Hindsgaul
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 650 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0968-0896
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The C-5 substituted uridine derivatives UDP-5-propylamine (7) and UDP-GlcNAc-5-propylamine (8) were synthesized in good yields by Heck alkylation of the 5-mercuriuridines, followed by hydrogenation. The products were characterized by 1H and 13C NMR spectroscopy, electrospray mass spectrometry and UV
## Terpenes U 0200 Synthesis of the Reported Structure (I) of Pogostol and a Total Synthesis of (Β±)-Kessane (II) without the Use of Protecting Groups. -(BOOKER-MILBURN\*, K. I.;
then treated with petroleum ether. This affords 0.26g (32 %) ( 5 a ) , m.p. 293-294Β°C. 0.31 g (38%) ( 3 a ) can be obtained from the petroleum ether solution by distillation.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.