Abstract
AbstractWith annual production at >85 million tons/year, ethanol is the world's largest‐volume renewable small molecule carbon source, yet its use as a C2‐feedstock in enantioselective C−C coupling is unknown. Here, the first catalytic enantioselective C−C couplings of ethanol are demonstrated in reactions with structurally complex, nitrogen‐rich allylic acetates incorporating the top 10 N‐heterocycles found in FDA‐approved drugs.
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