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- W3181106104 endingPage "1590" @default.
- W3181106104 startingPage "1565" @default.
- W3181106104 abstract "Olefin double-bond functionalization has been established as an excellent strategy for the construction of elaborate molecules. In particular, the hydroalkylation of olefins represents a straightforward strategy for the synthesis of new C(sp 3 )–C(sp 3 ) bonds, with concomitant formation of challenging quaternary carbon centers. In the last 20 years, numerous hydroalkylation methodologies have emerged that have explored the diverse reactivity patterns of the olefin double bond. This review presents examples of olefins acting as electrophilic partners when coordinated with electrophilic transition-metal complexes or, in more recent approaches, when used as precursors of nucleophilic radical species in metal hydride hydrogen atom transfer reactions. This unique reactivity, combined with the wide availability of olefins as starting materials and the success reported in the construction of all-carbon C(sp 3 ) quaternary centers, makes hydroalkylation reactions an ideal platform for the synthesis of molecules with increased molecular complexity." @default.
- W3181106104 created "2021-07-19" @default.
- W3181106104 creator A5018614924 @default.
- W3181106104 creator A5064926059 @default.
- W3181106104 date "2021-07-07" @default.
- W3181106104 modified "2023-10-16" @default.
- W3181106104 title "Methodologies for the synthesis of quaternary carbon centers via hydroalkylation of unactivated olefins: twenty years of advances" @default.
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