Asymmetric syntheses of (−)-methyl shikimate and (−)-5a-carba-β-d-gulopyranose from d-arabinose via Mukaiyama-type intramolecular aldolization
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Add time:08/21/2019 Source:sciencedirect.com
New asymmetric syntheses of (−)-methyl shikimate 1 and (−)-5a-carba-β-d-gulopyranose 11 from d-arabinose through a common route which employed Mukaiyama-type intramolecular aldolization as a key step were described.
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