An expedient synthesis of polyoxamic acid by a one-carbon masked acid addition to a glycoside aldehyde

Article abstract of DOI:10.1080/00397919908086024

The complete synthesis of a protected polyoxamic acid (14) from L- arabinose by the addition of an ortho-thioester nucleophile to appropriately protected L-threose aldehyde (7), is described.

Full text of DOI:10.1080/00397919908086024

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Synthetic Communications: An
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An Expedient Synthesis of
Polyoxamic Acid by a One-Carbon
Masked Acid Addition to a Glycoside
Aldehyde
Kristina M. K. Kutterer a & George Just b
a Steacie Institute for Molecular Sciences, National Research
Council of Canada , 100 Sussex Drive, Ottawa, Ontario,
Canada , KIA OR6
b McGill University , 801 Sherbrooke St. W., Montreal,
Quebec, Canada , H3A 2K6
Published online: 17 Sep 2007.
To cite this article: Kristina M. K. Kutterer & George Just (1999) An Expedient Synthesis of
Polyoxamic Acid by a One-Carbon Masked Acid Addition to a Glycoside Aldehyde, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic Organic
Chemistry, 29:21, 3841-3853, DOI: 10.1080/00397919908086024
To link to this article: http://dx.doi.org/10.1080/00397919908086024
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