A Divergent Synthesis of (+)-Muscarine and (+)-epi-Muscarine from d-Glucose
✍ Scribed by Velimir Popsavin; Ostoja Berić; Mirjana Popsavin; Ljubica Radić; János Csanádi; Vera Ćirin-Novta
- Book ID
- 108370885
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 207 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Stereospecific Synthesis of (-)-allo-Muscarine from D-Glucose: Novel Routes to the Key Chiral Synthon. -A simple and convenient four-step conversion of L-idose (I), which is readily available from D-glucose, to key intermediate (VI) in the (-)-allo-muscarine (VII) synthesis is described. Compared t
In the previous papers 1)2) concerning the synthesis of muscarines, we reported a partially stereospecific synthesis in which the hydroxyl group of a diacid (I) was introduced selectively in trans manner to the methyl group. Decarboxylation of I, however , proceeded non-stereoselectively giving a m
## 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.