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- W3092184504 endingPage "9157" @default.
- W3092184504 startingPage "9151" @default.
- W3092184504 abstract "Pd-catalyzed annulative couplings of 2-alkenylanilines with aldehydes using alcohols as both the solvent and hydrogen source have been developed. These domino processes allow divergent syntheses of two significant N-heterocycles, indoles and quinolines, from the same substrate by tuning reaction parameters, which seems to invoke two distinct mechanisms. The nature of the ligand and alcoholic solvent had a profound influence on the selectivity and efficiency of these protocols. Particularly noteworthy is that indole formation was achieved by overcoming two significant challenges, regioselective hydropalladation of alkenes and subsequent reactions between the resulting Csp3–Pd species and less reactive imines." @default.
- W3092184504 created "2020-10-15" @default.
- W3092184504 creator A5011861620 @default.
- W3092184504 creator A5046489294 @default.
- W3092184504 creator A5064501803 @default.
- W3092184504 date "2020-10-13" @default.
- W3092184504 modified "2023-10-17" @default.
- W3092184504 title "Divergent Syntheses of Indoles and Quinolines Involving N1–C2–C3 Bond Formation through Two Distinct Pd Catalyses" @default.
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