Download C-C Bond Activation by Guangbin Dong PDF

By Guangbin Dong

The sequence subject matters in present Chemistry provides serious stories of the current and destiny traits in smooth chemical study. The scope of insurance is all components of chemical technology together with the interfaces with similar disciplines equivalent to biology, drugs and fabrics technology. The objective of every thematic quantity is to offer the non-specialist reader, even if in academia or undefined, a accomplished perception into a space the place new learn is rising that's of curiosity to a bigger clinical viewers. each one assessment in the quantity seriously surveys one point of that subject and areas it in the context of the quantity as a complete. the main major advancements of the final five to ten years are provided utilizing chosen examples to demonstrate the foundations mentioned. The insurance isn't really meant to be an exhaustive precis of the sector or comprise huge amounts of information, yet should still otherwise be conceptual, focusing on the methodological pondering that may enable the non-specialist reader to appreciate the knowledge offered. Contributions additionally provide an outlook on power destiny advancements within the box. evaluation articles for the person volumes are invited by means of the amount editors. Readership: study chemists at universities or in undefined, graduate students

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Several alkyl–phenyl alkynes were also examined (alkyl¼Me, t-Bu, CF3; dippe, dtbpe, dippdmae), but only trifluoromethylphenylacetylene underwent Caryl–CC activation [62]. (27) 5 C–C Cleavage of Aryl–CH3 Bonds One other system in which substantial mechanistic work has been done on sp2–sp3 C–C activation is the rhodium pincer complexes that Milstein has investigated. The first discovery of this class of activation was made when he tried to attach a chelating phosphine to Rh(I). The chelate was found to undergo initial C–H activation, but continued heating under hydrogen led to cleavage of the methyl–aryl bond and loss of methane (28).

As mentioned above, the presence of Lewis acidic additives, such as triorganoaluminums and -aluminums, are known to facilitate the oxidative addition of C–CN bonds to nickel(0) species through the coordination of the nitrogen atom of cyano group to the Lewis acids [14, 38]. The arylcyanation of alkynes is indeed significantly accelerated by using aluminum-based Lewis acid cocatalysts (Scheme 25) [80, 81]. By cooperative nickel/Lewis acid catalysis, the scope of aryl cyanides has been improved to include those having labile bromo and chloro groups as well as sterically demanding substrates.

4 Cycloaddition Reactions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 Cyanation Reactions via C–CN Bond Activation . . . . . . . . . . . . . . . . . . . . . 1 Cyanation of Aryl Halides and Arenes . . . . . . . . . . . . . . . . . . . . . . . . 2 Carbocyanation of Unsaturated Bonds . . . . . . . . . . . . . . . .

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