Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 2, Pages 172-173Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b107817h
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A simple and practical method to make chiral propargylic alcohols has been developed: in the presence of a titanium alkoxide catalyst prepared in situ from titanium tetraisopropoxide and (R)-H-8-binaphthol, a variety of aromatic aldehydes were converted to the corresponding chiral propargylic alcohols with very good enantioselectivities (up to 96.2% e.e.) and yields.
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