Enantiospecific Synthesis of Protected 4-Deoxy-L-threose and 4-Deoxy-L-erythrose via Diastereoselective Reduction of L-Lactic Acid-derived Ketones

DOI: 10.1039/c39860000136

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Journal of the Chemical Society. Chemical communications p. 136 - 138 (1986)

Update date:2022-08-02

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Authors:

Guanti, Giuseppe

Banfi, Luca

Narisano, Enrica

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Article abstract of DOI:10.1039/c39860000136

The title compounds were synthesized from L-lactic acid via an acylation-reduction sequence employing lithium bis-p-tolylthiomethanide as a formyl anion equivalent.

Full text of DOI:10.1039/c39860000136

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