New Copper, Palladium and Nickel Catalytic Systems: An Evolution towards More Efficient Procedures

Metal‐catalysed reactions are a fundamental tool in synthetic chemistry. Increasingly challenging transformations can be accomplished only by means of certain metal catalysts. However, there still remains the need for a substantial decrease of the amount of catalyst, for better reuse or recycling of...

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Bibliographic Details
Published inChemical record Vol. 16; no. 3; pp. 1082 - 1095
Main Authors SanMartin, Raul, Herrero, María Teresa, Domínguez, Esther
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.06.2016
Wiley Subscription Services, Inc
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Summary:Metal‐catalysed reactions are a fundamental tool in synthetic chemistry. Increasingly challenging transformations can be accomplished only by means of certain metal catalysts. However, there still remains the need for a substantial decrease of the amount of catalyst, for better reuse or recycling of such active species, and for the avoidance of relatively toxic solvents in favour of environmentally friendly media. These facts apply to copper‐, palladium‐, and nickel‐catalysed cross‐coupling reactions, direct arylations, and oxidative processes. This account summarises our research on the last reactions, featuring an evolution towards more sustainable procedures in this field. Efficiency is the key: A summary of the development of new metal‐catalyzed arylation (O‐, S‐, and N‐arylations; α‐arylation of ketone enolates; Suzuki biaryl coupling; direct arylation of (hetero)arenes) and oxidation procedures, with a focus on catalyst loadings and more sustainable reagents/reaction media, is presented.
Bibliography:istex:5DD2C42CEDC882510F2DDFFBF52262DE928CC641
ArticleID:TCR201500289
ark:/67375/WNG-XTK3RJ2L-Q
Dedicated to Professor Timothy C. Gallagher on the occasion of his 60th birthday
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ISSN:1527-8999
1528-0691
DOI:10.1002/tcr.201500289