𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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


ChemInform Abstract: Stereospecific Synt
✍ V. POPSAVIN; O. BERIC; M. POPSAVIN; J. CSANADI; S. LAJSIC; D. MILJKOVIC 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

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

A simple, stereospecific synthesis of DL
✍ Takeshi Matsumoto; Akitami Ichihara; Noriki Itŏ 📂 Article 📅 1968 🏛 Elsevier Science 🌐 French ⚖ 151 KB

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