Matches in SemOpenAlex for { <https://semopenalex.org/work/W4241901400> ?p ?o ?g. }
- W4241901400 endingPage "9765" @default.
- W4241901400 startingPage "9758" @default.
- W4241901400 abstract "Abstract A photoredox‐catalyzed iminoalkenylation of γ‐alkenyl O‐acyl oximes has been developed. Readily available alkenylboronic acids serve as alkenylation reagents, leading to densely functionalized pyrrolines. Both ( E )‐ and ( Z )‐cinnamylpyrrolines are accessible depending on the reaction solvent. In dichloromethane, ( E )‐cinnamylpyrrolines are produced through a photoredox‐mediated single‐electron‐transfer process. In tetrahydrofuran, ( Z )‐cinnamylpyrrolines are generated by photocatalytic contra‐thermodynamic E ‐to‐ Z isomerization of ( E )‐cinnamylpyrrolines though an energy‐transfer pathway. Two stereocenters are established with complete diastereoselectivity and only one diastereomer is isolated." @default.
- W4241901400 created "2022-05-12" @default.
- W4241901400 creator A5004034857 @default.
- W4241901400 creator A5005804645 @default.
- W4241901400 creator A5007936773 @default.
- W4241901400 creator A5047309887 @default.
- W4241901400 date "2021-03-10" @default.
- W4241901400 modified "2023-10-18" @default.
- W4241901400 title "Diastereoselective and Stereodivergent Synthesis of 2‐Cinnamylpyrrolines Enabled by Photoredox‐Catalyzed Iminoalkenylation of Alkenes" @default.
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