Published 2010
by RSC Pub. in Cambridge .
Written in
Edition Notes
Includes bibliographical references and index.
| Statement | Hélène Pellissier |
| Series | RSC catalysis series -- no. 3, RSC catalysis series -- no. 3. |
| Classifications | |
|---|---|
| LC Classifications | QD505 . P465 2010 |
| The Physical Object | |
| Pagination | xv, 241 p. : |
| Number of Pages | 241 |
| ID Numbers | |
| Open Library | OL25224431M |
| ISBN 10 | 1849730547 |
| ISBN 10 | 9781849730549 |
| LC Control Number | 2012359901 |
| OCLC/WorldCa | 540182462 |
The aim of this book is to cover the very recent developments in asymmetric organocatalysis, focussing on those published since the beginning of The last decade has witnessed an explosive growth in the field of asymmetric organocatalysis wit. Organocatalysis in the synthesis of natural products: Recent developments in aldol and Mannich reactions, and 1,4-conjugated additions: 15COCT Recent progress in the Horner-Wadsworth-Emmons reaction, particularly, in its use for the synthesis of natural products: 15COC Print book: EnglishView all editions and formats Summary: An up-to-date digest on the rapidly expanding field of asymmetric organocatalysis, covering developments from . Introduction: Organocatalysis The catalysis with small organic molecules, where an inorganic element is not part of the active principle, has become a highly dynamic area in chemical research. Re-markably though, while several special issues in various journals, book .
Get this from a library! Recent developments in asymmetric organocatalysis. [Hélène Pellissier] -- An up-to-date digest on the rapidly expanding field of asymmetric organocatalysis, covering developments from onwards and aimed at organic chemists. The aim of this book is to cover the very. Last Friday, March 8th, Dr. Luca Bernardi (University of Bologna) visited Zaragoza and gave us a wonderful talk as a present, about “Asymmetric Organocatalysis: Principles and . Introduction. Regular achiral organocatalysts are based on nitrogen such as piperidine used in the Knoevenagel condensation. DMAP used in esterfications and DABCO used in the Baylis-Hillman reaction. Thiazolium salts are employed in the Stetter catalysts and reactions have a long history but current interest in organocatalysis is focused on asymmetric catalysis with chiral. Radical and Ion-pairing Strategies in Asymmetric Organocatalysis (Green Chemistry and Organcatalysts) - Kindle edition by Vitale, Maxime R, Oudeyer, Sylvain, Levacher, Vincent, Briere, Jean-Francois. Download it once and read it on your Kindle device, PC, phones or tablets. Use features like bookmarks, note taking and highlighting while reading Radical and Ion-pairing Strategies in Asymmetric Manufacturer: ISTE Press - Elsevier.
Recent Advances in Guanidine-Based Organocatalysts in Stereoselective Organic Transformation Reactions the historical landmark in the field of asymmetric catalysis was witnessed with the onset of asymmetric organocatalysis. Chiral motifs bearing organic molecules derived from nature’s chiral pool such as amino acids have been designed and. Organocatalysis has recently attracted enormous attention as green and sustainable catalysis. It was realized as a fundamental field providing wide families of catalysts for important organic transformations. It will certainly develop in the future. Given the diversity of accessible transformations, metal-catalyzed reactions have become major tools in organic synthesis that will undoubtedly. Part of the Green Chemistry and Sustainable Technology book series (GCST) Abstract. Chiral non-racemic epoxides are often endowed with important biological activities, but most of all, they are fundamental building blocks, frequently involved in the synthesis of natural and non-natural products, drugs and agrochemicals. Recent developments. The First Asymmetric Examples! The initial development of N-aryl-bicyclic triazoliums led the way to improved catalyst efficiency Rovisr, T. Chem. Lett. , 37, N NN X R1 n R2 Tunable electronics catalytic activity basicity Tunable sterics catalytic activity asymmetric induction.
