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- W3107189132 abstract "This chapter covers the hydroamination of unactivated alkenes, as well as of the slightly activated vinyl arenes, allenes, and 1,3-dienes. The hydroamination reactions of unactivated alkenes, although thermodynamically feasible under normal conditions, have a negative entropy. The lanthanides have sparked great interest for asymmetric synthesis since they were first used as enantioselective catalysts for Diels–Alder reactions. In 2014, Yang and coworkers reported the development of a novel amido-indenyl chiral yttrium complex capable of catalyzing the enantioselective intramolecular hydroamination of alkenes. Although palladium is a catalyst of excellence, making possible many chemical transformations, examples of palladium-catalyzed enantioselective hydroamination of alkenes appear to be restricted to intermolecular reactions. A much more versatile and active metal, which has been described as catalyzing several enantioselective intramolecular hydroamination reactions, is gold. Gold has been particularly useful in catalyzing reactions of allenes." @default.
- W3107189132 created "2020-12-07" @default.
- W3107189132 creator A5007816130 @default.
- W3107189132 creator A5027464254 @default.
- W3107189132 creator A5063013653 @default.
- W3107189132 date "2020-10-29" @default.
- W3107189132 modified "2023-10-15" @default.
- W3107189132 title "Synthesis of Five‐Membered <i>N</i> ‐Heterocycles by Enantioselective, Metal‐Catalyzed, Intramolecular Hydroamination of Alkenes" @default.
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