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Direct, highly enantioselective pyrrolidine sulfonamide catalyzed Michael addition of aldehydes to nitrostyrenes
Wei Wang
, Jian Wang, Hao Li
Research output
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Article
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peer-review
379
Scopus citations
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Dive into the research topics of 'Direct, highly enantioselective pyrrolidine sulfonamide catalyzed Michael addition of aldehydes to nitrostyrenes'. Together they form a unique fingerprint.
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Keyphrases
Enantioselectivity
100%
Aldehydes
100%
Michael Addition
100%
Pyrrolidine
100%
Sulfonamides
100%
Nitrostyrene
100%
Ketones
50%
Michael Addition Reaction
50%
Thiol-Michael Addition
50%
Mannich Reaction
50%
Organocatalyst
50%
Nitroolefins
50%
Enantioselective Michael Addition
50%
Aminoxylation
50%
Chemistry
Michael Addition
100%
Pyrrolidine
100%
Sulfonamide
100%
Addition Reaction
50%
Ketones
50%
Organocatalyst
50%
Nitroolefin
50%