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Koch, Florian M., Peters, René (2007) Catalytic Enantio- and Diastereoselective Formation of β-Sultones: Ring-Strained Precursors for Enantioenriched β-Hydroxysulfonyl Derivatives. Angewandte Chemie International Edition, 46 (15). 2685-2689 doi:10.1002/anie.200604796

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Reference TypeJournal (article/letter/editorial)
TitleCatalytic Enantio- and Diastereoselective Formation of β-Sultones: Ring-Strained Precursors for Enantioenriched β-Hydroxysulfonyl Derivatives
JournalAngewandte Chemie International Edition
AuthorsKoch, Florian M.Author
Peters, RenéAuthor
Year2007 (April 2)Volume46
Issue15
PublisherWiley
DOIdoi:10.1002/anie.200604796Search in ResearchGate
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Mindat Ref. ID8580081Long-form Identifiermindat:1:5:8580081:8
GUID0
Full ReferenceKoch, Florian M., Peters, René (2007) Catalytic Enantio- and Diastereoselective Formation of β-Sultones: Ring-Strained Precursors for Enantioenriched β-Hydroxysulfonyl Derivatives. Angewandte Chemie International Edition, 46 (15). 2685-2689 doi:10.1002/anie.200604796
Plain TextKoch, Florian M., Peters, René (2007) Catalytic Enantio- and Diastereoselective Formation of β-Sultones: Ring-Strained Precursors for Enantioenriched β-Hydroxysulfonyl Derivatives. Angewandte Chemie International Edition, 46 (15). 2685-2689 doi:10.1002/anie.200604796
In(2007, April) Angewandte Chemie International Edition Vol. 46 (15) Wiley

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Koch, Florian M., Peters, René (2007) Katalytische enantio- und diastereoselektive Synthese von β-Sultonen: ringgespannte Vorstufen für enantiomerenangereicherte β-Hydroxysulfonylderivate. Angewandte Chemie, 119 (15). 2739-2743 doi:10.1002/ange.200604796
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
Zhang, Jun‐Hao, Xu, Hui, Tang, Xiaodong, Dang, Yanfeng, Zhang, Fa‐Guang, Ma, Jun‐An (2023) Highly Enantio‐ and Diastereoselective Hydrogenation of Cyclic Tetra‐Substituted β‐Enamido Phosphorus Derivatives. Angewandte Chemie International Edition, 62 (28) doi:10.1002/anie.202305315
Llamas, Tomás, Arrayás, Ramón Gómez, Carretero, Juan C. (2007) Catalytic Asymmetric Conjugate Reduction of β,β-Disubstituted α,β-Unsaturated Sulfones. Angewandte Chemie International Edition, 46 (18). 3329-3332 doi:10.1002/anie.200700296
Zajac, Marian, Peters, René (2009) Catalytic Asymmetric Synthesis of β-Sultams as Precursors for Taurine Derivatives. Chemistry - A European Journal, 15 (33). 8204-8222 doi:10.1002/chem.200900496
Howard, James K., Müller, Marion, Berry, Alan, Nelson, Adam (2016) An Enantio- and Diastereoselective Chemoenzymatic Synthesis of α-Fluoro β-Hydroxy Carboxylic Esters. Angewandte Chemie International Edition, 55 (23). 6767-6770 doi:10.1002/anie.201602852
Desrosiers, Jean-Nicolas, Charette, André B. (2007) Catalytic Enantioselective Reduction of β,β-Disubstituted Vinyl Phenyl Sulfones by Using Bisphosphine Monoxide Ligands. Angewandte Chemie International Edition, 46 (31). 5955-5957 doi:10.1002/anie.200701367
Barluenga, José, Álvarez-Gutiérrez, Julia M., Ballesteros, Alfredo, González, José M. (2007) Directortho Iodination of β- and γ-Aryl Alkylamine Derivatives. Angewandte Chemie International Edition, 46 (8). 1281-1283 doi:10.1002/anie.200603631
Ortín, Irene, Dixon, Darren J. (2014) Direct Catalytic Enantio- and Diastereoselective Mannich Reaction of Isocyanoacetates and Ketimines. Angewandte Chemie International Edition, 53 (13). 3462-3465 doi:10.1002/anie.201309719
Huang, Haoxi, Peters, René (2009) A Highly Strained Planar-Chiral Platinacycle for Catalytic Activation of Internal Olefins in the Friedel-Crafts Alkylation of Indoles. Angewandte Chemie International Edition, 48 (3). 604-606 doi:10.1002/anie.200804944
Zu, Liansuo, Li, Hao, Xie, Hexin, Wang, Jian, Jiang, Wei, Tang, Yun, Wang, Wei (2007) Synthesis of Highly Functionalized Chiral Cyclopentanes by Catalytic Enantio- and Diastereoselective Double Michael Addition Reactions. Angewandte Chemie International Edition, 46 (20). 3732-3734 doi:10.1002/anie.200700485
 
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