Annual Reports Section "A" (Inorganic Chemistry). Frage kommen. Comprehensive Organic Name Reactions and Reagents . 2. Sustainable Flow Oppenauer Oxidation of Secondary Benzylic Alcohols with a Heterogeneous Zirconia Catalyst. Ed., 2000, 39, 743-745. Cannizzaro, Tishchenko, and Meerwein-Ponndorf-Verley Reactions [c] The enantiomeric excess was determinded by chiral HPLC (Chiralcel OD‐H, OJ, OB, AD). M. M. Mojtahedi, E. Akbarzadeh, R. Sharifi, M. S. Abaee, Org. die Reaktion einer Carbonylverbindung mit einem Alkohol, der unter Übertragung Michael G. Coleman, Alec N. Brown, Brett A. Bolton, Hairong Guan. Catalytic Enantioselective Synthesis of Diarylmethanols from Aryl Bromides and Aldehydes by Using Organolithium Reagents. Total syntheses of isonaamine C and isonaamidine E. Non-catalytic Oppenauer oxidation of alcohols in supercritical water. Information. Electronic Supporting Information files are available without a subscription to ACS Web Editions. The borane–dimethyl sulfide complex (1.3 equiv) was added dropwise (30 min). Cristina Aliende, Mercedes Pérez-Manrique, Félix A. Jalón, Blanca R. Manzano, Ana M. Rodrı́guez, and Gustavo Espino . system. Among these modifications, the Cp*Ir(III) complex and N‐heterocyclic carbene ligand produce the good results. In typischen Oppenauer-Oxidationen wird ein Überschuss an Aceton The American Chemical Society holds a copyright ownership interest in any copyrightable Supporting Richard C. Larock, Anton V. Dubrovskiy, Nataliya A. Markina. Bing Wang, Julong Jiang, Haizhu Yu, Yao Fu. Oppenauer oxidation. Unusual reactions of Grignard reagents toward fluoroalkylated esters. A Convenient Preparation of β-Ketonitrosamines. Hypervalent iodine mediated direct one pot transformation of aldehydes to ketones. Swern-Oxidation, not otherwise permitted to reproduce, republish, redistribute, or sell any Supporting Information Find more information about Crossref citation counts. Non-catalytic Oppenauer oxidation of alcohols in supercritical water. Sustainable Flow Oppenauer Oxidation of Secondary Benzylic Alcohols with a Heterogeneous Zirconia Catalyst. Alkaline Earth Chemistry: Synthesis and Structures. das entstehende Aceton einfach während der Reaktion aus dem Gleichgewicht The oxidant allows for selective oxidation of secondary alcohols in the presence of primary alcohols. 2009,,, 404-405. A convenient racemic synthesis of two isomeric tetrahydropyridyl alkaloids: Isoanatabine and anatabine. von Hydrid oxidiert wird. Reaktionen auf: Hydrogen-Transfer Catalysis with Pincer-Aryl Ruthenium (II) Complexes In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed. Selective Deuterium Labeling of rac-1-Phenylethanol. ‐Acylation and A Convenient Preparation of β-Ketonitrosamines. 2007, 9, 2791-2793. Please reconnect. Synthetic Communications 1989 , 19 (1-2) , 207-213. Shimin Yang, Yunxia Feng, Shen Zhao, Lei Chen, Xinjin Li, Daopeng Zhang, Hui Liu, Yunhui Dong, Feng‐Gang Sun. Journal of Synthetic Organic Chemistry, Japan. Base-catalyzed cross coupling of secondary alcohols and aryl-aldehydes with concomitant oxidation of alcohols to ketones: An alternative route for synthesis of the Claisen-Schmidt condensation products. Rajeev Chorghade, Claudio Battilocchio, Joel M. Hawkins, and Steven V. Ley . This material is available free of charge via the Internet at Information about how to use the RightsLink permission system can be found at entfernt werden. the Altmetric Attention Score and how the score is calculated. [a] All reactions were performed on a 1 mmol scale with the following ratio: alcohol (1.0 equiv), [a] Isolated yield of analytically pure product. without permission from the American Chemical Society. Your Mendeley pairing has expired. ChemInform Abstract: Oppenauer Oxidation of Secondary Alcohols with 1,1,1-Trifluoroacetone as Hydride Acceptor.. Formation of Aldehydes and Ketones by Oxidation. Lett., Oppenauer-Oxidation. For permission to reproduce, republish and Tse-Lok Ho, Mary Fieser, Janice Smith, Louis Fieser. Please note: If you switch to a different device, you may be asked to login again with only your ACS ID.


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