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Synlett 1992; 1992(12): 969-971
DOI: 10.1055/s-1992-21548
DOI: 10.1055/s-1992-21548
letter
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Synthetic Studies on the 1-Hydroxy Nortropane System,-Part III:1 Total Enantioselective Synthesis of (-)-Calystegine B2
Further Information
Publication History
Publication Date:
08 March 2002 (online)
(-)-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.