Download C-C Bond Activation by Guangbin Dong PDF

Organic

By Guangbin Dong

ISBN-10: 3642550541

ISBN-13: 9783642550546

The sequence subject matters in present Chemistry offers serious experiences of the current and destiny traits in smooth chemical learn. The scope of insurance is all components of chemical technological know-how together with the interfaces with comparable disciplines resembling biology, drugs and fabrics technology. The target of every thematic quantity is to offer the non-specialist reader, no matter if in academia or undefined, a accomplished perception into a space the place new learn is rising that's of curiosity to a bigger medical viewers. each one overview in the quantity seriously surveys one point of that subject and locations it in the context of the quantity as an entire. the main major advancements of the final five to ten years are awarded utilizing chosen examples to demonstrate the rules mentioned. The assurance isn't really meant to be an exhaustive precis of the sector or contain huge amounts of information, yet may still otherwise be conceptual, targeting the methodological pondering that may permit the non-specialist reader to appreciate the knowledge offered. Contributions additionally provide an outlook on capability destiny advancements within the box. evaluation articles for the person volumes are invited via the quantity editors. Readership: learn chemists at universities or in undefined, graduate students

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Extra resources for C-C Bond Activation

Sample text

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

Y. jp 35 37 37 39 41 43 43 44 44 55 56 34 Y. 2]octane Diisobutylaluminum hydride 1,2-Dimethoxyethane Dimethylformamide 1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone Bis(diphenylphosphino)butane Bis(diphenylphosphino)ethane Enantiomer excess Equivalent(s) Ethyl Hour(s) Isopropyl Methyl Mesityl 2,4,6-trimethylphenyl (not methanesulfonyl) Phenyl Phenanthroline Phthalate Pinacolato Propyl Room temperature 2-Dicyclohexylphosphino-20 ,60 -dimethoxybiphenyl tert-Butyldimethylsilyl tert-Butyl Tetrahydrofuran N,N,N0 ,N0 -Tetramethylethylenediamine Trimethylsilyl Turnover number Tosyl 4-toluenesulfonyl 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene Catalytic C–CN Bond Activation 35 1 Introduction Nitriles are common and ubiquitous organic compounds.

4 Summary, Conclusions, Outlook . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Y. jp 35 37 37 39 41 43 43 44 44 55 56 34 Y. 2]octane Diisobutylaluminum hydride 1,2-Dimethoxyethane Dimethylformamide 1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone Bis(diphenylphosphino)butane Bis(diphenylphosphino)ethane Enantiomer excess Equivalent(s) Ethyl Hour(s) Isopropyl Methyl Mesityl 2,4,6-trimethylphenyl (not methanesulfonyl) Phenyl Phenanthroline Phthalate Pinacolato Propyl Room temperature 2-Dicyclohexylphosphino-20 ,60 -dimethoxybiphenyl tert-Butyldimethylsilyl tert-Butyl Tetrahydrofuran N,N,N0 ,N0 -Tetramethylethylenediamine Trimethylsilyl Turnover number Tosyl 4-toluenesulfonyl 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene Catalytic C–CN Bond Activation 35 1 Introduction Nitriles are common and ubiquitous organic compounds.

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