Recent advances in palladium-catalyzed (hetero)annulation of CC bonds with ambiphilic organo(pseudo)halides
Palladium has proven to be effective in catalyzing the (hetero)annulation of CC 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 CC bond v...
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| Published in | Chemical communications (Cambridge, England) Vol. 57; no. 62; pp. 7610 - 7624 |
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| Main Authors | , , |
| Format | Journal Article |
| Language | English |
| Published |
Cambridge
Royal Society of Chemistry
03.08.2021
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| Abstract | Palladium has proven to be effective in catalyzing the (hetero)annulation of CC 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 CC 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. |
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| AbstractList | Palladium has proven to be effective in catalyzing the (hetero)annulation of CC 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 CC 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. Palladium has proven to be effective in catalyzing the (hetero)annulation of 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=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. |
| Author | Cooper, Phillippa Engle, Keary M. Ni, Hui-Qi |
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| Snippet | Palladium has proven to be effective in catalyzing the (hetero)annulation of CC bonds with ambiphilic organo(pseudo)halides. Through the employment of... Palladium has proven to be effective in catalyzing the (hetero)annulation of C=C bonds with ambiphilic organo(pseudo)halides. Through the employment of... |
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| SubjectTerms | Alkenes catalytic activity chemical communication Chemical reactions couplings Dienes Halides Organic chemistry Palladium strains styrene Styrenes |
| Title | Recent advances in palladium-catalyzed (hetero)annulation of CC bonds with ambiphilic organo(pseudo)halides |
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