Matches in SemOpenAlex for { <https://semopenalex.org/work/W3174769949> ?p ?o ?g. }
- W3174769949 endingPage "6340" @default.
- W3174769949 startingPage "6334" @default.
- W3174769949 abstract "Efficient access to two enantiomers of one chiral compound is critical for the discovery of drugs. However, it is still a challenging problem owing to the difficulty in obtaining two enantiomers of one chiral catalyst. Here, we report a general method to obtain both enantiomeric products via fine tuning the hydrogen-bonding interactions of phosphonium salts. Amino acid derived phosphonium salts and dipeptide derived phosphonium salts exhibited different properties for controlling the transition state, which could efficiently promote the Michael addition reaction to give opposite configurations of products with high yields and enantioselectivities. Preliminary investigations on the mechanism of the reaction and applications of the products were also performed." @default.
- W3174769949 created "2021-07-05" @default.
- W3174769949 creator A5031899206 @default.
- W3174769949 creator A5041745232 @default.
- W3174769949 creator A5050103767 @default.
- W3174769949 creator A5052550377 @default.
- W3174769949 creator A5065208984 @default.
- W3174769949 date "2021-01-01" @default.
- W3174769949 modified "2023-09-25" @default.
- W3174769949 title "Enantioselectivity switch in asymmetric Michael addition reactions using phosphonium salts" @default.
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