Synthetic Studies on the 1-Hydroxy Nortropane System,-Part III:1Total Enantioselective Synthesis of (-)-Calystegine B2
- 1 January 1992
- journal article
- letter
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 1992 (12) , 969-971
- https://doi.org/10.1055/s-1992-21548
Abstract
(-)-Calystegine B2 {8-azabicyclo[3.2.1]octane-1,2,3,4-tetraol} was prepared from D-glucose via Ferrier reaction, regiospecific ring enlargement of a polysubstituted cyclohexanone and intramolecular cyclisation of 4-aminocycloheptanone.Keywords
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