Recent advances in palladium-catalyzed (hetero)annulation of C![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) C bonds with ambiphilic organo(pseudo)halides
C bonds with ambiphilic organo(pseudo)halides                                                    
    
                    Abstract
Palladium has proven to be effective in catalyzing the (hetero)annulation of C![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) C bonds with ambiphilic organo(pseudo)halides. Through the employment of appropriate ambiphilic coupling partners, efficient annulation of a variety of allenes, 1,3-dienes, strained alkenes, styrenes, and other C
C bonds with ambiphilic organo(pseudo)halides. Through the employment of appropriate ambiphilic coupling partners, efficient annulation of a variety of allenes, 1,3-dienes, strained alkenes, styrenes, and other C![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) C bond variants can be achieved to provide direct access to numerous useful hetero- and carbocyclic scaffolds. In this Feature Article, we summarize palladium-catalyzed (hetero)annulation methods reported since 2005 (spanning just over 15 years) and discuss outstanding challenges in this area of study.
C bond variants can be achieved to provide direct access to numerous useful hetero- and carbocyclic scaffolds. In this Feature Article, we summarize palladium-catalyzed (hetero)annulation methods reported since 2005 (spanning just over 15 years) and discuss outstanding challenges in this area of study.
- This article is part of the themed collection: 2021 Emerging Investigators
 
                




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        ![[double bond, length as m-dash]](https://www.rsc.org/images/entities/h2_char_e001.gif) C bonds with ambiphilic organo(pseudo)halides
C bonds with ambiphilic organo(pseudo)halides