N-Heterocyclic Carbenes in Transition Metal Catalysis, Frank Glorius

Автор: Jie Jack Li
Название: Palladium in Heterocyclic Chemistry,26
ISBN: 0080451179 ISBN-13(EAN): 9780080451176
Издательство: Elsevier Science
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Описание: Intends to highlight important palladium-mediated reactions of heterocycles with emphasis on the unique characteristics of individual heterocycles. This book comprises a compilation of important preparations of heteroaryl halides, boranes and stannanes for each heterocycle.

Автор: Alan R. Katritzky
Название: Handbook of Heterocyclic Chemistry,
ISBN: 0080958435 ISBN-13(EAN): 9780080958439
Издательство: Elsevier Science
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Описание: Heterocyclic compounds play a vital role in the metabolism of living cells. Their practical applications range from extensive clinical use to fields as diverse as agriculture, photography, biocide formulation and polymer science. This book covers the structure, reactivity and synthesis of various heterocyclic compounds.

Автор: Li, Jie Jack
Название: Name reactions in heterocyclic chemistry II
ISBN: 0470085088 ISBN-13(EAN): 9780470085080
Издательство: Wiley
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Описание: Co-authored by Nobel Laureatte, E.J. Corey, this book builds on the first volume on this topic by presenting a comprehensive treatise on name reactions in heterocyclic chemistry.

Автор: Chen
Название: New Strategies for N-Heterocyclic Carbenes Catalyzed Annulations
ISBN: 9811028982 ISBN-13(EAN): 9789811028984
Издательство: Springer
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Описание: This thesis focuses on NHC-catalyzed annulation of nitroalkenes, enals and ?,?-unsaturated carboxylic acids. (1) NHCs were found to be efficient catalysts for the [4+2] annulation of ?-substituted nitroalkenes. The scope of Rauhut–Currier reaction was successfully extended to the most challenging ?-substituted alkenes by this method; (2) Enals were successfully used for [4+2] annulations with azodicarboxylates catalyzed by NHC via ?-addition. Highly enantiopure tetrahydropyridazinones and ?-amino acid derivatives could be easily prepared by subsequent transformations of the resulting dihydropyridazinones. (4) The readily available ?,?-unsaturated carboxylic acids were first successfully employed to generate the ?,?-unsaturated acyl azolium intermediates by using NHC for the enantioselective [3+2] and [3+3] annulations.