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Kull, Thomas, Peters, René (2008) Contact Ion Pair Directed Lewis Acid Catalysis: Asymmetric Synthesis oftrans‐Configured β‐Lactones. Angewandte Chemie International Edition, 47 (29). 5461-5464 doi:10.1002/anie.200801143

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Reference TypeJournal (article/letter/editorial)
TitleContact Ion Pair Directed Lewis Acid Catalysis: Asymmetric Synthesis oftrans‐Configured β‐Lactones
JournalAngewandte Chemie International Edition
AuthorsKull, ThomasAuthor
Peters, RenéAuthor
Year2008 (July 7)Volume47
Issue29
PublisherWiley
DOIdoi:10.1002/anie.200801143Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID8585570Long-form Identifiermindat:1:5:8585570:2
GUID0
Full ReferenceKull, Thomas, Peters, René (2008) Contact Ion Pair Directed Lewis Acid Catalysis: Asymmetric Synthesis oftrans‐Configured β‐Lactones. Angewandte Chemie International Edition, 47 (29). 5461-5464 doi:10.1002/anie.200801143
Plain TextKull, Thomas, Peters, René (2008) Contact Ion Pair Directed Lewis Acid Catalysis: Asymmetric Synthesis oftrans‐Configured β‐Lactones. Angewandte Chemie International Edition, 47 (29). 5461-5464 doi:10.1002/anie.200801143
In(2008, July) Angewandte Chemie International Edition Vol. 47 (29) Wiley

See Also

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Kull, Thomas, Cabrera, José, Peters, René (2010) Catalytic Asymmetric Synthesis of trans-Configured β-Lactones: Cooperation of Lewis Acid and Ion Pair Catalysis. Chemistry - A European Journal, 16 (30). 9132-9139 doi:10.1002/chem.201000840
Kull, Thomas, Peters, René (2008) Kontaktionenpaar‐gesteuerte Lewis‐Säurekatalyse zur asymmetrischen Synthese vontrans‐konfigurierten β‐Lactonen. Angewandte Chemie, 120 (29). 5541-5544 doi:10.1002/ange.200801143
Tiseni, Paolo S., Peters, René (2007) Catalytic Asymmetric Formation of δ-Lactones by [4+2] Cycloaddition of Zwitterionic Dienolates Generated from α,β-Unsaturated Acid Chlorides. Angewandte Chemie International Edition, 46 (28). 5325-5328 doi:10.1002/anie.200700859
Bera, Srikrishna, Samanta, Ramesh C., Daniliuc, Constantin G., Studer, Armido (2014) Asymmetric Synthesis of Highly Substituted β-Lactones through Oxidative Carbene Catalysis with LiCl as Cooperative Lewis Acid. Angewandte Chemie International Edition, 53 (36). 9622-9626 doi:10.1002/anie.201405200
Bera, Srikrishna, Samanta, Ramesh C., Daniliuc, Constantin G., Studer, Armido (2014) Corrigendum: Asymmetric Synthesis of Highly Substituted β-Lactones through Oxidative Carbene Catalysis with LiCl as Cooperative Lewis Acid. Angewandte Chemie International Edition, 53 (45). 12005 doi:10.1002/anie.201409589
Rueping, Magnus, Sugiono, Erli, Merino, Estíbaliz (2008) Asymmetric Iminium Ion Catalysis: An Efficient Enantioselective Synthesis of Pyranonaphthoquinones and β-Lapachones. Angewandte Chemie International Edition, 47 (16). 3046-3049 doi:10.1002/anie.200705110
Jautze, Sascha, Peters, René (2008) Enantioselective Bimetallic Catalysis of Michael Additions Forming Quaternary Stereocenters. Angewandte Chemie International Edition, 47 (48). 9284-9288 doi:10.1002/anie.200803539
Wang, Xingwang, List, Benjamin (2008) Asymmetric Counteranion-Directed Catalysis for the Epoxidation of Enals. Angewandte Chemie International Edition, 47 (6). 1119-1122 doi:10.1002/anie.200704185
Peters, René (2010) Chiral Ferrocenes in Asymmetric Catalysis. Synthesis and Applications. Edited by Li-Xin Dai and Xue-Long Hou. Angewandte Chemie International Edition, 49 (25). 4163-4164 doi:10.1002/anie.201001671
Denmark, Scott E., Beutner, Gregory L. (2008) Lewis Base Catalysis in Organic Synthesis. Angewandte Chemie International Edition, 47 (9). 1560-1638 doi:10.1002/anie.200604943
Fischer, Daniel F., Peters, René (2009) Acid Catalysis in Modern Organic Synthesis.1+2. Edited by Hisashi Yamamoto and Kazuaki Ishihara. Angewandte Chemie International Edition, 48 (4). 640 doi:10.1002/anie.200805065
 
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