Issue 21, 1976
From the journal:

Journal of the Chemical Society, Chemical Communications

Synthesis of one enantiomer, the other enantiomer, and a mixture of both enantiomers of frontalin from a derivative of methyl-α-D-glucopyranoside

David R. Hicks  and  Bert Fraser-Reid  

Abstract

The ketone (1), derivable from methyl-α-D-glucopyranoside in four steps, may be converted into one enantiomer, the other enantiomer, or a mixture of both enantiomers of frontalin in 13% overall yield.

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Article information

DOI
https://doi.org/10.1039/C39760000869
Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 869-870

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Synthesis of one enantiomer, the other enantiomer, and a mixture of both enantiomers of frontalin from a derivative of methyl-α-D-glucopyranoside

D. R. Hicks and B. Fraser-Reid, J. Chem. Soc., Chem. Commun., 1976, 869 DOI: 10.1039/C39760000869

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