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1976•Journal of the Chemical Society Chemical CommunicationsRequires access

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

DAVID ROY HICKS, Bert Fraser‐Reid

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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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What this paper is about

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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OpenAlex reports 25 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available 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.

Key concepts: Enantiomer, Chemistry, Yield (engineering), Derivative (finance), Ketone, Stereochemistry, Methyl Ketone, Organic chemistry

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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 — Research Paper | ScholarLens