The title glycosides were synthesised from D-glUCOSe, via the common intermediate methyl 2-acetamido-4-O-benzoyld-bromo-2,3,6-trideoxy-a-D-ribohexopyranoside . \*To whom enquiries should be addressed. \*\*The overall efficiency of this procedure can be improved by using a phase-transfer process' in
โฆ LIBER โฆ
The synthesis of 3-acetamido-2,3,5,6-tetradeoxy-5-fluoro-d,l-ribo-hexofuranose by the direct fluorination of methyl 3-acetamido-2,3,6-trideoxy-d,l-arabino-hexopyranoside (methyl N-acetyl-d,l-acosaminide)
โ Scribed by John T. Welch; Britt-Marie Svahn; Seetha Eswarakrishnan; John P. Hutchinson; Jon Zubieta
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 671 KB
- Volume
- 132
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Syntheses of methyl 2,6-diacetamido-2,3,
โ
Mohammed M. Abuaan; John S. Brimacombe; Leslie C.N. Tucker
๐
Article
๐
1984
๐
Elsevier Science
๐
English
โ 612 KB
ChemInform Abstract: Studies of the Synt
โ
H. YE; L. NOECKER; W. J. BOYKO; R. M. GIULIANO; G. P. A. YAP; A. L. RHEINGOLD
๐
Article
๐
2010
๐
John Wiley and Sons
โ 31 KB
๐ 2 views
Studies of the Synthesis of Rubranitrose and Crystal Structure of Methyl 2,3,6-Trideoxy-3-C-methyl-3-nitro-ฮฑ-D-ribo-hexopyranoside. -The title hexopyranoside (II) is investigated as a precursor to D-rubranitrose, a nitro sugar found in the antibiotic rubradirin. -(YE, H.; NOECKER,
Synthesis of the deculopyranosonic acid
โ
Heinz-Werner Hagedorn; Hans Merten; Reinhard Brossmer
๐
Article
๐
1992
๐
Elsevier Science
๐
English
โ 772 KB
ChemInform Abstract: Syntheses of Methyl
โ
Philip G. Hultin; Ryan M. Buffie
๐
Article
๐
2010
๐
John Wiley and Sons
โ 39 KB
๐ 1 views
ChemInform Abstract: Bromohydroxylation
โ
Gaik B. Kok; Tho van Phan; Mark von Itzstein
๐
Article
๐
2010
๐
John Wiley and Sons
โ 37 KB
๐ 3 views
The synthesis, and study of the ฮฒ-elimin
โ
Hari G. Garg; Roger W. Jeanloz
๐
Article
๐
1979
๐
Elsevier Science
๐
English
โ 995 KB
2-Acetamido-3,4,6-tri-U-acetyl-2-deoxy-a-~-glucopyranosyl chloride was condensed with the iV-(benzyloxycarbonyl) derivatives of,