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https://doi.org/10.1021/cs4002332
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Cite Journal: ACS Catalysis |  Publication Date: May 20, 2013 |
 Citations: 62 |
The asymmetric intramolecular oxa-Michael reactions of α,β-unsaturated ketones have been achieved by using readily accessible primary–secondary diamines as the organocatalysts, giving the synthetically useful tetrahydrofurans/2H-pyrans in good yields and with high enantioselectivities (up to 90% ee).
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