4.8 Article

Asymmetric One-Pot Synthesis of 1,3-Oxazolidines and 1,3-Oxazinanes via Hemiaminal Intermediates

Journal

ORGANIC LETTERS
Volume 16, Issue 16, Pages 4098-4101

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol501789c

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Funding

  1. National Institutes of Health [NIH GM-082935]
  2. National Science Foundation [NSF-0847108]

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A highly efficient method for the enantioselective one-pot synthesis of 1,3-oxazolidines and 1,3-oxazinanes has been reported. The reaction proceeds via the formation of hemiaminal intermediates obtained by the enantioselective addition of respective alcohols to imines catalyzed by a chiral magnesium phosphate catalyst, followed by intramolecular cyclization under mildly basic conditions. A wide range of substrates have been converted to the respective chiral heterocyclic products in high yields and with excellent enantioselectivities using this one-pot procedure.

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