Download C-C Bond Activation by Guangbin Dong PDF

By Guangbin Dong

The sequence subject matters in present Chemistry offers serious stories of the current and destiny tendencies in smooth chemical learn. The scope of insurance is all parts of chemical technology together with the interfaces with similar disciplines comparable to biology, medication and fabrics technological know-how. The aim of every thematic quantity is to provide the non-specialist reader, even if in academia or undefined, a entire perception into a space the place new examine is rising that's of curiosity to a bigger clinical viewers. each one overview in the quantity seriously surveys one point of that subject and locations it in the context of the amount as a complete. the main major advancements of the final five to ten years are offered utilizing chosen examples to demonstrate the foundations mentioned. The insurance isn't meant to be an exhaustive precis of the sphere or comprise huge amounts of information, yet should still otherwise be conceptual, targeting the methodological considering that may permit the non-specialist reader to appreciate the data awarded. Contributions additionally provide an outlook on capability destiny advancements within the box. assessment articles for the person volumes are invited via the amount editors. Readership: study chemists at universities or in undefined, graduate students

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Here, if the PMe2 groups are replaced with PPh2 groups, C–H activation of the methyl group occurs, but there is no rearrangement to the C–C cleavage product as seen in (28). 25:1), with eventual formation of only the C–C insertion product [65]. 75:1), but the C–H insertion product must be heated to induce rearrangement to the C–C insertion product. Since the C–H insertion product does not convert into the C–C insertion product under the reaction conditions, it is not an intermediate in the C–C cleavage mechanism.

Coupling Reactions via C–CN Bond Activation . . . . . . . . . . . . . . . . . . . . . . 1 Hydrodecyanation Reactions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Cross-Coupling Reactions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 Silylation and Borylation Reactions . . . . . . . . . . . . . . . . . . . . . . . . . . 4 Cycloaddition Reactions .

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. The reaction conditions of allylcyanation can also 48 Y. Nakao Scheme 25 Aryl- and allylcyanation of alkynes catalyzed cooperatively by nickel/aluminum Scheme 26 Total synthesis of plaunotol through allylcyanation of alkynes be made milder by using AlMe2Cl as a Lewis acid cocatalyst, allowing highly stereoselective preparation of tri-substituted alkenes bearing a bulkier substituent at the cyano-substituted carbon [82].

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