Journal
CHEMICAL COMMUNICATIONS
Volume 52, Issue 72, Pages 10882-10885Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6cc04096a
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Funding
- National Natural Science Foundation of China [21372220, 21532006]
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A highly enantioselective addition of arylboronic acids to cyclic alpha-ketiminophosphonates is reported using a chiral palladium phos-phinooxazoline catalyst, providing an efficient and facile route to quaternary alpha-aminophosphonates in high yields and up to 99.9% enantioselectivity.
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