Journal
ORGANIC LETTERS
Volume 24, Issue 2, Pages 714-719Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c04157
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Funding
- National Natural Science Foundation of China [82188101, 21725205, 21432007, 21572246, 21702223]
- Key-Area Research and Development Program of Guangdong Province [2020B010188003]
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Highly enantioselective hydrogenation of (Z)-N-sulfonyl-α-dehydroamido boronic esters using a JosiPhos-type ligand is realized for the first time. This method enables the convenient synthesis of a series of enantio-enriched N-sulfonyl-α-amido boronic esters with good yields and excellent enantioselectivities (up to 99% ee).
Highly enantioselective rhodium-catalyzed hydrogenation of (Z)-N-sulfonyl-alpha-dehydroamido boronic esters is realized for the first time using a JosiPhos-type ligand. This method has enabled convenient synthesis of a series of enantio-enriched N-sulfonyl-alpha-amido boronic esters in good yields and excellent enantioselectivities (up to 99% ee).
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