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- W2740254829 endingPage "415" @default.
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- W2740254829 abstract "Abstract The rhodium‐catalyzed 1,4‐addition of organoboron reagents to electron‐deficient alkenes is a versatile method for the enantioselective construction of carbon–carbon bonds. The scope of these reactions is broad, and alkenes activated by adjacent carbonyls, imines, nitriles, phosphonyl groups, nitro groups, sulfonyl groups, C=N‐containing aromatic heterocycles, electron‐deficient arenes, or boryl groups are effective substrates. Regarding the pronucleophilic component, aryl‐, heteroaryl‐, and alkenylboron reagents have been successfully employed. In addition, numerous chiral ligands have been developed which impart high enantioselectivities onto these reactions. Importantly, these reactions usually proceed under mild, experimentally convenient conditions, with no requirement for precautions to exclude air or moisture. This chapter presents the scope and limitations of this process, along with a discussion of the current understanding of the mechanistic and stereochemical features. Incorporation of this process into domino reactions is discussed, as is its application in the synthesis of biologically active molecules. The literature is covered up until the end of 2013." @default.
- W2740254829 created "2017-08-08" @default.
- W2740254829 creator A5012353194 @default.
- W2740254829 creator A5020935313 @default.
- W2740254829 creator A5072023551 @default.
- W2740254829 date "2017-08-01" @default.
- W2740254829 modified "2023-10-16" @default.
- W2740254829 title "Enantioselective, Rhodium‐Catalyzed 1,4‐Addition of Organoboron Reagents to Electron‐Deficient Alkenes" @default.
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