Popsavin et al., 1995 - Google Patents
An alternative synthesis of (+)-epiallo-muscarine from D-glucosePopsavin et al., 1995
View PDF- Document ID
- 729953112739081935
- Author
- Popsavin V
- Berić O
- Popsavin M
- Csanádi J
- Miljković D
- Publication year
- Publication venue
- Carbohydrate research
External Links
Snippet
Preparation of muscarine and its analogues in optically pure form has attracted considerable interest mainly due to their marked biological activity [1]. Several syntheses of muscarine stereoisomers have been achieved so far [2], including the synthesis of (+)-epiallo …
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