By Peter I. Dalko

A much-needed evaluation reflecting the advancements during the last 5 years, this can be the main accomplished instruction manual on organocatalysis. As such, all suitable catalyst platforms are mentioned intimately, in addition to key concepts, response forms, and demanding functions in overall synthesis. the 1st volumes hide catalyst constructions and fundamental activation forms. those chapters let readers to familiarize themselves with the rather complicated interactions that make organocatalytic reactions selective; to achieve an perception into the most productive catalyst kinds; and to appreciate the significance of actual parameters that impact reactivity and selectivity. quantity 3 is based round response kinds, i.e. nucleophile additions to C=X and C=C bonds; Friedel-Crafts reactions, organocatalytic sigmatropic reactions, regioselective reactions and desymmetrization ideas, ring-forming reactions, multicomponent (domino) reactions, multicatalyst structures and the appliance of organocatalytic reactions in multistep synthesis are mentioned. An appendix recollecting catalyst buildings with the enough cross-references to the corresponding chapters rounds off the book.
With its contributions written by means of pioneers of the organocatalysis box, this e-book offers non-specialists with an advent to the subject in addition to serving as a precious resource for researchers in academia and looking for an up to date and complete assessment of this promising quarter of artificial natural chemistry.

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Extra resources for Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications, 3 Volume Set

Sample text

17 Finally, it has been shown that thiourea-type bifunctional catalysts are also useful for asymmetric aldol reactions [234, 235] and α-chlorination of aldehydes [236]. Furthermore, 4-substituted bifunctional analogs have been developed for use in anti-selective Mannich reactions [237]. 7 Miscellaneous As described so far, various pyrrolidine-based chiral organocatalysts open the door to a remarkably fruitful world of synthetic chemistry. In general, the synthetic protocol used to design new catalysts relies on the naturally occurring chiral source L-proline (1) as a key component.

Moscow 119991 Russia Piotr Kwiatkowski University of Warsaw Faculty of Chemistry Pasteura 1 02-093 Warsaw Poland Aitor Landa The University of the Basque Country (UPV-EHU) Department of Organic Chemistry I Manuel Lardizabal, 3 20018 Donostia-San Sebastián Spain Guilong Li University of South Florida Department of Chemistry 4202 East Fowler Avenue CHE205A Tampa, FL 33613 USA Saihu Liao Shanghai Institute of Organic Chemistry State Key Laboratory of Organometallic Chemistry 345 Lingling Lu Shanghai 200032 China Rosa López The University of the Basque Country (UPV-EHU) Department of Organic Chemistry I Manuel Lardizabal, 3 20018 Donostia-San Sebastián Spain Yixin Lu Hangzhou Normal University Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education Hangzhou 310012 China and National University of Singapore Department of Chemistry 3 Science Drive 3 Singapore 117543 Republic of Singapore Dawid Łyz˙wa University of Warsaw Faculty of Chemistry Pasteura 1 02-093 Warsaw Poland XXXVI List of Contributors Rainer Mahrwald Humboldt-University Institute of Chemistry Brook-Taylor Str.

In these examples, to gain satis­ factory results, it is important to match the chirality between the proline core and the attachment. O TBSO N N CO2Et H O ‡ CO2Et O H H R 15 Several other related systems containing a prolinamide or proline-thioamide core have also been reported [36–42]. In some cases, a chiral diamine assembly can serve as an effective scaffold for the design of multiply functionalized catalysts like 11 and 12 [43–49]. Proline hydrazides [50], dipeptides [51–57], or other small peptides [58–63] bearing a prolinamide core have been shown to be useful in asymmetric aldol reactions.

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