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- W3080370595 endingPage "10636" @default.
- W3080370595 startingPage "10627" @default.
- W3080370595 abstract "Developing tandem multiple C–H substitution reactions of simple alkenes provides rapid access to structurally complex unsaturated building blocks. Amidomethylative reactions that reserve C═C double bonds have been composed sequentially for tandem catalytic substitutions around the C═C bonds of alkenes. As a proof-of-concept demonstration, tandem catalytic amidomethylative processes, which effectively form multiple C–C bonds, have been developed to directly and selectively transform α-substituted styrenes into unsaturated N-heterocycles. Using Fe(OTf)3 as the sole catalyst, the operationally simple protocols employ bench-stable bisamidomethane as the sole reagent to produce hexahydropyrimidines and 1,2,3,6-tetrahydropyridine derivatives. Moreover, the practical catalytic processes constituted facile two-step pathways, from simple α-substituted styrenes, to access unsaturated 1,3-diamine and bispidine derivatives." @default.
- W3080370595 created "2020-09-01" @default.
- W3080370595 creator A5006391667 @default.
- W3080370595 creator A5012528047 @default.
- W3080370595 creator A5016118278 @default.
- W3080370595 creator A5018268684 @default.
- W3080370595 creator A5023377350 @default.
- W3080370595 creator A5031977438 @default.
- W3080370595 creator A5037614116 @default.
- W3080370595 creator A5081380948 @default.
- W3080370595 creator A5082252890 @default.
- W3080370595 date "2020-08-25" @default.
- W3080370595 modified "2023-10-16" @default.
- W3080370595 title "Fe(III)-Based Tandem Catalysis for Amidomethylative Multiple Substitution Reactions of α-Substituted Styrene Derivatives" @default.
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