Synthesis of spiro[pyrido[3,2-b][1,4]oxazin-2,2′-pyrans] based upon methyld-arabino-2-hexulopyranosonate
✍ Scribed by Jens Andersch; Dieter Sicker; Horst Wilde
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 123 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The novel glycosyl donor 1, derived from methyl D-arabino.2-hextdopyranosoante, was transformed into glycoside 2, diastereoselectively. Catalytic hydrogenation of 2 and spontaneous reductive cyclization gave access to the spiro[pyridol3,2-bl[l,4loxazin-2,2'-pyrm~ i 3 and 4.
📜 SIMILAR VOLUMES
## Abstract Dedicated to Professor Klaus Burger on the occasion of his 60th birthday Methyl β‐D‐__arabono__‐2‐hexulopyranosonate 1 has __via__ the novel glycosyl donor 3 been transformed into the thiophenyl glycosides 4 and 5. Catalytic hydrogenation of the nitro compound 4 in alkaline solution led
## Synthesis of Spiro[1,4-benzothiazine-2,2'-pyrans] Starting from Methyl β-D-arabino-2-Hexulopyranosonate. -Based on sugar (I), the cyclic hydroxamic acid (VI) and the lactams (VIII) and (IX) are prepared via the thiophenyl glycosides (V) and (VII). The spirobenzothiazinepyrans (VI), (VIII), and
## 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