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- W2950374623 endingPage "538" @default.
- W2950374623 startingPage "532" @default.
- W2950374623 abstract "Abstract A new silver(I) triflate‐promoted tandem reaction comprising the ring opening of aziridines and a Michael reaction has been developed. Using secondary amines or primary amines as nucleophiles, this methodology allows for the synthesis of cis ‐1‐alkyl‐4‐aminotetrahydroisoquinolines or cis ‐1,3‐disubstituted isoindolines in good yields with excellent diastereoselectivities, respectively. Besides, easy operation and mild reaction conditions are also notable features of this tandem reaction. magnified image" @default.
- W2950374623 created "2019-06-27" @default.
- W2950374623 creator A5004961918 @default.
- W2950374623 creator A5008038973 @default.
- W2950374623 creator A5009724342 @default.
- W2950374623 creator A5016414843 @default.
- W2950374623 creator A5068595048 @default.
- W2950374623 creator A5076250804 @default.
- W2950374623 date "2016-01-26" @default.
- W2950374623 modified "2023-10-18" @default.
- W2950374623 title "Diastereoselective Synthesis of Substituted Tetrahydroisoquinolines and Isoindolines<i>via</i>a Silver(I) Triflate-Promoted Tandem Reaction" @default.
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