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Publications and Patents
Diplomandenstellen in Stuttgart
Die Gruppe Peters zieht zum 01.10.2008 an die Universität Stuttgart!
Motivierte Chemiestudenten mit ausgeprägter Leidenschaft für synthetische organische Chemie, Metallorganik und Katalyse, die Interesse haben an einer Diplomarbeit in der Gruppe Peters, werden gebeten sich zu bewerben. Bitte kontaktieren Sie für weitere Details und Themenvorschläge peters@org.chem.ethz.ch
- S. Jautze, R. Peters,* Angew. Chem. Int. Ed. 2008, 47, asap.
Bimetallic Enantioselective Catalysis of Michael Additions Forming Quaternary Stereocenters.
Angew. Chem. 2008, 120, asap.
Enantioselektive Dimetallkatalyse von Michael-Additionen zur Bildung quartärer Stereozentren.
- R. Peters,* D. F. Fischer, S. Jautze, F. M. Koch, T. Kull, P. S. Tiseni, Z.-q. Xin, M. Zajac, Chimia 2008, 62, 497-505.
Catalytic Methods for Direct Access to Chiral High-Added-Value Products.
- T. Kull, R. Peters,* Angew. Chem. Int. Ed. 2008, 47, 5431-5464.
Contact Ion Pair Directed Lewis Acid Catalysis: Asymmetric Synthesis of trans-Configured β-Lactones.
Angew. Chem. 2008, 120, 5541-5544.
Kontaktionenpaar-gesteuerte Lewis-Säurekatalyse zur asymmetrischen Synthese von trans-konfigurierten β-Lactonen.
- F. M. Koch, R. Peters,* Synlett 2008, 1505-1509.
Rapid Asymmetric Access to β-Hydroxysulfinic Acids and Allylsulfonic Acids by Chemoselective Reduction of β-Sultones.
- Z.-q. Xin, D. F. Fischer, R. Peters,* Synlett 2008, 1495-1499.
Catalytic Asymmetric Formation of Secondary Allylic Amines by Aza-Claisen Rearrangement of Trifluoroacetimidates.
- P. S. Tiseni, R. Peters,* Org. Lett. 2008, 10, 2019-2022.
Lewis Acid-Lewis Base Catalyzed Enantioselective Hetero-Diels-Alder Reaction for Direct Access to delta-Lactones.
- S. Jautze, P. Seiler, R. Peters,* Chem. Eur. J. 2008, 14, 1430-1444.
Synthesis of Nearly Enantiopure Allylic Amines by Aza-Claisen Rearrangement of Z-Configured Allylic Trifluoroacetimidates Catalyzed by Highly Active Ferrocenylbispalladacycles.
- D. F. Fischer, Z.-q. Xin, R. Peters,* Angew. Chem. Int. Ed. 2007, 46, 7704-7707;
Asymmetric Formation of Allylic Amines with N-Substituted Quaternary Stereocenters by PdII-Catalyzed Aza-Claisen Rearrangements.
Angew. Chem. 2007, 119, 7848-7851.
Asymmetrische Synthese von Allylaminen mit N-substituierten quartären Stereozentren durch Palladium(II)-katalysierte Aza-Claisen-Umlagerungen.
- T. Kull, R. Peters,* Adv. Synth. Catal. 2007, 349, 1647-1652.
Practical Enantioselective Synthesis of beta-Lactones Catalyzed by Aluminum Bissulfonamide Complexes.
- P. S. Tiseni, R. Peters,* Angew. Chem. Int. Ed. 2007, 46, 5325-5328;
Catalytic Asymmetric Formation of delta-Lactones by [4+2] Cycloaddition of Zwitterionic Dienolates Generated from alfa,beta-Unsaturated Acid Chlorides.
Angew. Chem. 2007, 119, 5419-5422.
Katalytische asymmetrische Synthese von delta-Lactonen durch [4+2]-Cycloaddition von zwitterionischen Dienolaten, erzeugt aus alfa,beta-ungesättigten Säurechloriden.
- M. Zajac, R. Peters,* Org. Lett. 2007, 9, 2007-2010.
Catalytic Asymmetric Formation of beta-Sultams.
- F. M. Koch, R. Peters,* Angew. Chem. Int. Ed. 2007, 46, 2685-2689;
Catalytic Enantio- and Diastereoselective Formation of beta-Sultones: Ring-Strained Precursors for Enantioenriched beta-Hydroxysulfonyl Derivatives.
Angew. Chem. 2007, 119, 2739-2743.
Katalytische enantio- und diastereoselektive Synthese von beta-Sultonen: ringgespannte Vorstufen für enantiomerenangereicherte beta-Hydroxysulfonylderivate.
- S. Jautze, P. Seiler, R. Peters,* Angew. Chem. Int. Ed. 2007, 46, 1260-1264;
Macrocyclic Ferrocenyl-Bisimidazoline Palladacycle Dimers as Highly Active and Enantioselective Catalysts for the Aza-Claisen Rearrangement of Z-Configured N-para-Methoxyphenyl Trifluoroacetimidates.
Angew. Chem. 2007, 119, 1282-1286.
Makrocyclische Ferrocenyl-Bisimidazolin-Palladacyclus-Dimere als hoch aktive und enantioselektive Katalysatoren für die Aza-Claisen-Umlagerung von Z-konfigurierten N-para-Methoxyphenyltrifluoracetimidaten.
- R. Peters,* C. Diolez, A. Rolland, E. Manginot, M. Veyrat, Heterocycles 2007, 72, 255-273.
Practical Racemic and Asymmetric Formal Total Syntheses of the Homocamptothecin Derivative and Anticancer Agent Diflomotecan via Tertiary Homoallylic Alcohols as Masked Aldol Equivalents.
- R. Peters,* M. Althaus, C. Diolez, A. Rolland, E. Manginot, M. Veyrat, J. Org. Chem. 2006, 71, 7583-7595.
Practical Formal Total Syntheses of the Homocamptothecin Derivative and Anticancer Agent Diflomotecan via Asymmetric Acetate Aldol Additions to Pyridine Ketone Substrates.
- R. Peters, PCT Int. Appl. 2006, US 2006189807.
Process for the manufacture of intermediates in camptothecin production.
- R. Peters,* D. F. Fischer, Angew. Chem. Int. Ed. 2006, 45, 5736-5739;
Total Syntheses of the Antibacterial Natural Product Abyssomicin C. (highlight article)
Angew. Chem. 2006, 118, 5866-5869.
Totalsynthesen des antibakteriellen Naturstoffes Abyssomicin C. (highlight article)
- M. E. Weiss, D. F. Fischer, Z.-q. Xin, S. Jautze, W. B. Schweizer, R. Peters,* Angew. Chem. Int. Ed. 2006, 45, 5694-5698;
Practical, Highly Active and Enantioselective Ferrocenyl-Imidazoline Palladacycle Catalysts (FIPs) for the Aza-Claisen Rearrangement of N-para-Methoxyphenyl Trifluoroacetimidates.
Angew. Chem. 2006, 118, 5823-5827.
Praktikable, hochaktive und enantioselektive Ferrocenyl-Imidazolin-Palladacyclus(FIP)-Katalysatoren für die Aza-Claisen-Umlagerung von N-para-Methoxyphenyltrifluoracetimidaten.
- F. Matsuura, R. Peters, M. Anada, S. S. Harried, J. Hao, Y. Kishi,*
J. Am. Chem. Soc. 2006, 128, 7463-7465.
Unified Total Synthesis of Pteriatoxins and Their Diastereomers.
- R. Peters,* Z.-q. Xin, D. F. Fischer, W. B. Schweizer, Organometallics 2006, 25. 2917-2920.
Synthesis and Diastereoselective ortho-Lithiation/Cyclopalladation of Enantiopure [2-Imidazolyl]-1',2',3',4',5'-pentamethylferrocenes and -1',2',3',4',5'-pentaphenylferrocenes.
- C. Diolez, E. Manginot, R. Peters,* A. Rolland, M. Veyrat, PCT Int. Appl. 2006, WO 2006033011.
Novel processes for the production of 3-(pyridin-4-yl)-3-hydroxypentanoic acid intermediates.
- R. Peters,* M. Althaus, A.-L. Nagy, Org. Biomol. Chem. 2006, 4, 498-509.
Practical formal total synthesis of (rac)- and (S)-camptothecin.
- R. Peters,* D. F. Fischer, Org. Lett. 2005, 7, 4137-4140.
Preparation and Diastereoselective Ortho-Metalation of Chiral Ferrocenyl Imidazolines: Remarkable Influence of LDA as Metalation Additive.
- R. Peters,* P. Waldmeier, A. Joncour, Org. Proc. Res. Dev. 2005, 9, 508-512.
Efficient Synthesis of a 5HT2c Receptor Agonist Precursor.
- A. Job, C. Janeck, W. Bettray, R. Peters, D. Enders,* Tetrahedron 2002, 58, 2253-2329.
SAMP – A Versatile Auxiliary in Asymmetric Synthesis.
- D. Enders,* R. Peters, R. Lochtman, G. Raabe, J. Runsink, J. W. Bats, Eur. J. Org. Chem. 2000, 3399-3426.
Asymmetric Synthesis of Novel Ferrocenyl Ligands with Planar and Central Chirality and their Application to Pd-Catalyzed Allylic Substitution.
- D. Enders,* R. Peters, R. Lochtman, J. Runsink, Eur. J. Org. Chem. 2000, 2839-2850.
Enantioselective Synthesis of Planar Chiral ortho-Functionalized Ferrocenylketones.
- D. Enders,* L. Wortmann, R. Peters, Acc. Chem. Res. 2000, 33, 157-169.
Recovery of Carbonyl Compounds from N,N-Dialkylhydrazones.
- D. Enders,* R. Peters, J. Runsink, J. W. Bats, Org. Lett. 1999, 1, 1863-1866.
Novel Ferrocenyl Ligands with Planar and Central Chirality in Pd-Catalyzed Allylic Substitutions.
- D. Enders,* R. Peters, R. Lochtman, G. Raabe, Angew. Chem. Int. Ed.1999, 38, 2421-2423;
Asymmetric Synthesis of Novel Ferrocenyl Ligands with Planar and Central Chirality.
Angew. Chem.1999, 111, 2579-2581.
Asymmetrische Synthese neuer planar- und zentral-chiraler Ferrocenylliganden.
- D. Enders,* R. Peters, R. Lochtman, J. Runsink, Synlett 1997, 1462-1464.
Enantioselective Synthesis of Planar Chiral ortho-Functionalised Ferrocenylketones.
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