## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Stereoselective synthesis of the 5′-aminofuranoside part of polyoxins via (3,3)-sigmatropic rearrangement of allylic thiocyanates
✍ Scribed by Jozef Gonda; Miroslava Martinková; Martin Walko; Eva Zavacká; Miloš Buděšı́nský; Ivana Cı́sařová
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 123 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
A stereoselective synthesis of the branched-chain sugar 3(S)-isothiocyanato-3-deoxy-3-Cvinyl glucose via (3,3)-sigmatropie rearrangement of allylie thiocyanates prepared from D-glucose is presented. The side chain at C-4 of the substrates 4-Z, 4-E and 8-E is not a decisive factor for stereocontrol i
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access the actual ChemInform Abstract, please click on HTML or PDF.