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Contact Data:  
 
Prof. Dr. René Peters
University of Stuttgart
Pfaffenwaldring 55
 
D-70569 Stuttgart
 
NWZ I, 6-301
+49 (0)711 685 64330
+49 (0)711 685 54330

 

Publications and Patents

 

Polynuclear Enantiopure Salen–Mesoionic Carbene Hybrid Complexes.
J. Schmid, W. Frey, R. Peters, Organometallics, DOI: 10.1021/acs.organomet.7b00729.

Ruthenium-Catalyzed Synthesis of 2H-Azirines from Isoxazolinones.
S. Rieckhoff, M. Titze, W. Frey, R. Peters, Org. Lett. 2017, 19, 4436–4439.

Titanium Salen Complexes with Appended Silver NHC Groups as Nucleophilic Carbene Reservoir for Cooperative Asymmetric Lewis Acid / NHC Catalysis.
K. Latendorf, M. Mechler, I. Schamne, D. Mack, W. Frey, R. Peters, Eur. J. Org. Chem. 2017, 28, 4140–4167.

An Aluminum Fluoride Complex with an Appended Ammonium Salt as an Exceptionally Active Cooperative Catalyst for the Asymmetric Carboxycyanation of Aldehydes
D. Brodbeck, F. Broghammer, J. Meisner, J. Klepp, D. Garnier, W. Frey, J.Kästner, R. Peters, Angew. Chem. Int. Ed. 2017, 56, 4056–4060.
Ein Aluminium-Fluorid-Komplex mit gekoppelter Ammonium-Einheit als außergewöhnlich aktiver kooperativer Katalysator in der asymmetrischen Carboxycyanierung von Aldehyden.

D. Brodbeck, F. Broghammer, J. Meisner, J. Klepp, D. Garnier, W. Frey, J.Kästner, R. Peters, Angew. Chem. 2017, 129, 4115–4119.

Cooperative Lewis acid–onium salt catalysis as tool for the desymmetrization of meso-epoxides.
F. Broghammer, D. Brodbeck, T. Junge, R. Peters, Chem. Commun. 2017, 53, 1156-1159.
open access

Highly Enantioselective Ferrocenyl Palladacycle-Acetate Catalysed Arylation of Aldimines and Ketimines with Arylboroxines.
C. Schrapel, W. Frey, D. Garnier, R. Peters, Chem. Eur. J. 2017, 23, 2448–2460.

Dual Palladium(II)/Tertiary Amine Catalysis for Asymmetric Regioselective Rearrangements of Allylic Carbamates.
J. M. Bauer, W. Frey, R. Peters, Chem. Eur. J. 2016, 22, 5767–5777.

Regioselective Asymmetric Allylic Alkylation Reaction of -Cyanoacet­ates Catalyzed by a Heterobimetallic Platina-/Palladacycle
M. Weiss, J. Holz, R. Peters, Eur. J. Org. Chem. 2016, 210-227.

Dinuclear planar chiral ferrocenyl gold(I) & gold(II) complexes.
M. Ayerbe Garcia, W. Frey, M. Ringenberg, M. Schwilk, R. Peters, Chem.Commun. 2015, 51, 16806-16809.
open access

Diastereodivergent Asymmetric 1,4-Addition of Oxindoles to Nitroolefins by Using Polyfunctional Nickel-Hydrogen-Bond-Azolium Catalysts.
M. Mechler, R. Peters, Angew. Chem. Int. Ed. 2015, 54, 10303–10307.
Diastereodivergente asymmetrische 1,4-Additionen von Oxindolen an Nitroolefine durch polyfunktionelle Nickel-H-Brücken-Azolium-Katalysatoren.
M. Mechler, R. Peters, Angew. Chem. 2015, 127, 10442–10446.

Exogenous-Base-Free Palladacycle-Catalyzed Highly Enantioselective Arylation of Imines with Arylboroxines.
C. Schrapel, R. Peters, Angew. Chem. Int. Ed. 2015, 54, 10289–10293.
Palladacyclus-katalysierte, hoch enantioselektive Arylierung von Iminen mit Arylboroxinen ohne Verwendung einer exogenen Base.
C. Schrapel, R. Peters, Angew. Chem. 2015, 127, 10428–10432.

Regioselective Pd-Catalyzed Synthesis of 2,3,6-Trisubstituted Pyridines from Isoxazolinones.
S. Rieckhoff, T. Hellmuth, R. Peters, J. Org. Chem. 2015, 80, 6822–6830.

Catalytic asymmetric [3,3]-rearrangements of allylic acetimidates.
J. M. Bauer, R. Peters, Catal. Sci. Technol. 2015, 5, 2340-2346.
open access

 

Regioselective Catalytic Asymmetric C-Alkylation of Isoxazolinones by a Base-Free Palladacycle-Catalyzed Direct 1,4-Addition.
T. Hellmuth, W. Frey, R. Peters, Angew. Chem. Int. Ed. 2015, 54, 2788–2791.
Regioselektive katalytische asymmetrische C-Alkylierung von Isoxazolinonen durch basenfreie Palladacyclus-katalysierte direkte 1,4-Addition.
T. Hellmuth, W. Frey, R. Peters, Angew. Chem. 2015, 127, 2829–2833.

 

Catalytic Direct Dehydrogenative Cross-Couplings of C−H (Pro)Nucleophiles and Allylic Alcohols without an Additional Oxidant.
M. Weiss, R. Peters, ACS Catal. 2015, 5, 310-316.

 

Bimetallic Catalysis: Cooperation of Carbophilic Metal Centers.
M. Weiss, R. Peters, in: Cooperative Catalysis – Designing Efficient Catalysts for Synthesis, R. Peters (Ed.), Wiley-VCH, Weinheim, 2015.

 

Cooperative Catalysis – Designing Efficient Catalysts for Synthesis.
R. Peters (Ed.), Wiley-VCH, Weinheim, 2015.

Heterogenization of ferrocene palladacycle catalysts on ROMP-derived monolithic supports and application to a Michael addition.
M. Sudheendran, S. H. Eitel, S. Naumann, M. R. Buchmeiser, R. Peters, New J. Chem. 2014, 38, 5597-5607.

 

Macrocyclic Salen−Bis-NHC Hybrid Ligands and Their Application to the Synthesis of Enantiopure Bi- and Trimetallic Complexes.
M. Mechler, W. Frey, R. Peters, Organometallics 2014, 33, 5492-5508.

Asymmetric Cascade Reaction to Allylic Sulfonamides from Allylic Alcohols by Palladium(II)/Base-Catalyzed Rearrangement of Allylic Carbamates.
J. M. Bauer, W. Frey, R. Peters, Angew. Chem. Int. Ed. 2014, 53, 7634-7638.
Asymmetrische Kaskadenreaktion zu Allylsulfonamiden aus Allylalkoholen über eine Palladium(II)/Base-katalysierte Umlagerung von Allylcarbamaten.
J. M. Bauer, W. Frey, R. Peters, Angew. Chem. 2014, 126, 7764-7768.

Succinimieds by a Tandem Sequence

Cooperative Bimetallic Asymmetric Catalysis: Comparison of a Planar Chiral Ruthenocene Bis-Palladacycle to the Corresponding Ferrocene.
T. Hellmuth, S. Rieckhoff, M. Weiss, K. Dorst, W. Frey, R. Peters, ACS Catal. 20144, 1850-1858.
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Author Profile René Peters.
R. Peters, Angew. Chem. Int. Ed2014, 53, 5499. 
Autorenprofil René Peters.
R. Peters, Angew. Chem. 2014, 126, 5604.

Sterically Demanding Planar Chiral P,N Ligands by Diastereoselective Ortho Lithiation of Pentaphenylferrocenyloxazolines and Their Application to Palladium-Catalyzed Substitutions with Cyclic Allylic Acetates.
M. Ayerbe Garcia, W. Frey, R. Peters, Organometallics 2014, 33, 1068-1078.
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Asymmetric Pd(II)-Catalyzed Cascade Reaction Giving Quaternary Amino Succinimides via 1,4-Addition and a Nef-Type-Reaction.
M. Weber, W. Frey, R. Peters, Angew. Chem. Int. Ed2013, 52, 13223-13227.
Asymmetrische Palladium(II)-katalysierte Kaskadenreaktion zu quartären Aminosuccinimiden über 1,4-Addition und eine Nef-artige Reaktion
M. Weber, W. Frey, R. Peters, Angew. Chem. 2013, 125, 13465-13469.

Succinimieds by a Tandem Sequence

Monomeric Ferrocene Bis-Imidazoline Bis-Palladacycles: Variation of Pd–Pd Distances by an Interplay of Metallophilic, Dispersive, and Coulombic Interactions.
M. Weber, J. E. M. N. Klein, B. Miehlich, W. Frey, R. Peters, Organometallics 2013, 32, 5810-5817.
Pd-Pd Distance in Ferrocene-Bis-Imidazolin-Bis-Palladaycles
Catalytic Asymmetric Synthesis of Spirocyclic Azlactones by a Double Michael Addition Approach.
M. Weber, W. Frey, R. Peters, Chem. Eur. J. 2013, 19, 8342-8351.
Enantioselective Spiro Azlacton Formation

Asymmetric Michael Additions of α-Cyanoacetates by Soft Lewis Acid / Hard Brønsted Acid Catalysis: Stereodivergency With Bi- vs Monometallic Catalysts.
S. H. Eitel, S. Jautze, W. Frey, R. Peters, Chem. Sci. 2013, 4, 2218-2233.

For reprints please contact: rene.peters@oc.uni-stuttgart.de


Simon3

Homo- and Hetero-Bimetallic Pd-, Ag- and Ni-Hybrid Salen―Bis-NHC Complexes.
M. Mechler, K. Latendorf, W. Frey, R. Peters, Organometallics 2013, 32, 112-130.
Oxidative Transmetallation
Pd(II)-Catalyzed Regio-, Enantio- and Diastereoselective 1,4-Addition of Azlactones Formed In-Situ From Racemic Unprotected Amino Acids and Acetic Anhydride.
M. Weber, R. Peters, J. Org. Chem. 2012, 77, 10846–10855.
PPFIP catalyzed 1,4-Addition
Asymmetric Synthesis of Hetero-Bimetallic Planar Chiral Ferrocene Pallada-/Platinacycles and their Application to Enantioselective Aza-Claisen Rearrangements.
M. Weiss, W. Frey, R. Peters, Organometallics 2012, 31, 6365–6372.
Pt/Pd cycle catalyzed Aza-Claisen
Bispalladacycle Catalyzed Michael Addition of In-Situ Formed Azlactones to Enones.
M. Weber, S. Jautze, W. Frey, R. Peters Chem. Eur. J. 2012, 18, 14792–14804.
Michael-Addition of In-Situ Formed Azlactones to Enones
Crystal structure of pentaphenylferrocenium tetrafluoroborate, C40H30BF4Fe.
W. Frey, S. H. Eitel, R. Peters, Z. Kristallogr. NCS 2012, 227, 559-561.
Crystal Structure
Cooperative Al(Salen)-Pyridinium Catalysts for the Asymmetric Synthesis of trans-Configured β-Lactones by [2+2]-Cyclocondensation of Acylbromides and Aldehydes: Investigation of Pyridinium Substituent Effects.
P. Meier, F. Broghammer, K. Latendorf, G. Rauhut, R. Peters, Molecules 2012, 17, 7121–7150. (Special Issue Asymmetric Catalysis).
open access
[2+2]-Cyclocondensation
Catalytic Asymmetric Synthesis of Functionalized α,α-Disubstituted α-Amino Acid Derivatives from Racemic Unprotected α-Amino Acids via In-Situ Generated Azlactones.
M. Weber, W. Frey, R. Peters, Adv. Synth. Catal. 2012, 354, 1443–1449.
Onepot-Five-Steps-Syntesis of Quaternary Amino Acids
Paramagnetic Palladacycles with PdIII Centers are Highly Active Catalysts for Asymmetric Aza-Claisen Rearrangements.
S. H. Eitel, M. Bauer, D. Schweinfurth, N. Deibel, B. Sarkar, H. Kelm, H.-J. Krüger, W. Frey, R. Peters, J. Am. Chem. Soc. 2012, 134, 4683–4693.
Pd(III) complexes
Isomerizations to Form a Stereogenic Center and Allylic Rearrangements.
S. Jautze, R. Peters, In Science of Synthesis: Stereoselective Synthesis, Evans, P. A.,
Ed.; Thieme: Stuttgart, 2011; Vol. 3, Chapter 3.10, pp 443–467.
Lewis Acid/Base Catalyzed [2+2]-Cycloaddition of Sulfenes and Aldehydes: A Versatile Entry to Chiral Sulfonyl and Sulfinyl Derivatives.
F. M. Koch, R. Peters, Chem. Eur. J. 2011, 17, 3679–3692.
Ferrocene and Half Sandwich Complexes as Catalysts with Iron Participation.
R. Peters, D. F. Fischer, S. Jautze, Top. Organomet. Chem.2011, 33, 139–175.
Bispalladacycle-Catalyzed Brønsted Acid/Base-Promoted Asymmetric Tandem Azlactone Formation−Michael Addition.
M. Weber, S. Jautze, W. Frey, R. Peters, J. Am. Chem. Soc. 2010, 132, 12222–12225.
Catalytic Asymmetric Synthesis of trans-Configured β-Lactones: Cooperation of Lewis Acid and Ion Pair Catalysis.
T. Kull, J. Cabrera, R. Peters, Chem. Eur. J. 2010, 16, 9132–9139.
Struktur41
Catalyst versus Substrate Induced Selectivity: Kinetic Resolution by Palladacycle Catalyzed Allylic Imidate Rearrangements.
R. Peters, Z.-q. Xin, F. Maier, Chem. Asian J. 2010, 5, 1770–1774.
Struktur
Synthesis of Densely Substituted Trans-Configured 4-Acylated Piperidine-2,4-diones as 3:1 Adducts of Imines and Ketenes.
J. Cabrera, T. Hellmuth, R. Peters, J. Org. Chem. 2010, 75, 4326–4329.
Struktur 38

Chiral Ferrocenes in Asymmetric Catalysis. Synthesis and Applications.(book review)
R. Peters, Angew. Chem. Int. Ed. 2010, 49, 4163–4164. Angew. Chem. 2010, 122, 4258.


Buch

Catalytic Asymmetric Formation of δ-Lactones from Unsaturated Acyl Halides.
P. S. Tiseni, R. Peters, Chem. Eur. J. 2010, 16, 2503–2517.
Struktur 36
Catalytic Asymmetric Michael Additions of α-Cyano Acetates.
S. Jautze, R. Peters, Synthesis 2010, 365–388.
Struktur 35

The Asymmetric Aza-Claisen Rearrangement: Development of Widely Applicable Pentaphenylferrocenyl Palladacycle Catalysts.
D. F. Fischer, A. Barakat, Z.-q. Xin, M. E. Weiss, R. Peters, Chem. Eur. J. 2009, 15, 8722–8741.
Struktur 34

Catalytic Asymmetric Synthesis of β-Sultams as Precursors for Taurine Derivatives.
M. Zajac, R. Peters, Chem. Eur. J. 2009, 15, 8204–8222.

Struktur 33

Diastereoselective Bis-Cyclopalladation of Ferrocene-1,1′-diyl
Bis-Imidazolines: Translation of Central via Axial into Planar Chirality
.

S. Jautze, S. Diethelm, W. Frey, R. Peters, Organometallics 2009, 28, 2001–2004.
Struktur 32

Acid Catalysis in Modern Organic Synthesis, Vol. 1+2.(book review).
D. F. Fischer, R. Peters, Angew. Chem. Int. Ed. 2009, 48, 640;
Angew. Chem. 2009, 121, 650.
Buchcover

A Highly Strained Planar Chiral Platinacycle for Catalytic Activation of Internal Olefins in the Friedel-Crafts Alkylation of Indoles.
H. Huang, R. Peters, Angew. Chem. Int. Ed. 2009, 48, 604–606.
Ein hoch-gespannter planar chiraler Platinacyclus zur katalytischen Aktivierung interner Olefine in Friedel-Crafts-Alkylierungen von Indolen.
Angew. Chem. 2009, 121, 612–615.

Struktur2

Bimetallic Enantioselective Catalysis of Michael Additions Forming Quaternary Stereocenters.
S. Jautze, R. Peters, Angew. Chem. Int. Ed. 2008, 47, 9284–9288;
Enantioselektive Dimetallkatalyse von Michael-Additionen zur Bildung quartärer Stereozentren.
Angew. Chem. 2008, 120, 9424–9429.
s3

Catalytic Methods for Direct Access to Chiral High-Added-Value Products.(account)
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.

Contact Ion Pair (CIP) Directed Lewis-Acid Catalysis: Asymmetric Formation of trans-Configured β-Lactones.
T. Kull, R. Peters, Angew. Chem. Int. Ed. 2008, 47, 5461–5464;
Kontaktionenpaar-gesteuerte Lewis-Säurekatalyse zur asymmetrischen Synthese von trans-konfigurierten β-Lactonen.
Angew. Chem. 2008, 120, 5541-5544.
s5

Rapid Asymmetric Access to β-Hydroxysulfinic Acids and Allylsulfonic Acids by Chemoselective Reduction of β-Sultones.
F. M. Koch, R. Peters, Synlett 2008, 1505–1509.
s6

 

Catalytic Asymmetric Formation of Secondary Allylic Amines by Aza-Claisen Rearrangement of Trifluoroacetimidates.
Z.-q. Xin, D. F. Fischer, R. Peters, Synlett 2008, 1495–1499.
s7

Lewis Acid-Lewis Base Catalyzed Enantioselective Hetero-Diels-Alder Reaction for Direct Access to δ-Lactones.
P. S. Tiseni, R. Peters, Org. Lett. 2008, 10, 2019–2022.
s8

Synthesis of nearly Enantiopure Allylic Amines by Aza-Claisen Rearrangement of Z-Configured Allylic Trifluoroacetimidates Catalyzed by Highly Active Ferrocenylbispalladacycles.
S. Jautze, P. Seiler, R. Peters, Chem. Eur. J. 2008, 14, 1430–1444.
s9

Asymmetric Formation of Allylic Amines with N-Substituted Quaternary Stereocenters by Pd(II)-Catalyzed Aza-Claisen Rearrangements.
D. F. Fischer, Z.-q. Xin, R. Peters, Angew. Chem. Int. Ed. 2007, 46, 7704-7707;
Asymmetrische Synthese von Allylaminen mit N-substituierten quartären Stereozentren durch Palladium(II)-katalysierte Aza-Claisen-Umlagerungen.
Angew. Chem. 2007, 119, 7848–7851.
s10

Practical Enantioselective Synthesis of β-Lactones Catalyzed by Aluminum Bissulfonamide Complexes.
T. Kull, R. Peters, Adv. Synth. Catal. 2007, 349, 1647–1652.
s11

Catalytic Asymmetric Formation of δ-Lactones by [4+2]-Cycloaddition of Zwitterionic Dienolates Generated from α,β-Unsaturated Acid Chlorides.
P. S. Tiseni, R. Peters, Angew. Chem. Int. Ed. 2007, 46, 5325-5328;
Katalytische asymmetrische Synthese von δ-Lactonen durch [4+2]-Cycloaddition von zwitterionischen Dienolaten, erzeugt aus α,β-ungesättigten Säurechloriden.
Angew. Chem. 2007, 119, 5419–5422.
s12a

Catalytic Asymmetric Formation of β-Sultams.
M. Zajac, R. Peters, Org. Lett. 2007, 9, 2007–2010.
s13

First Catalytic Enantio- and Diastereoselective Formation of β-Sultones: Ring-Strained Precursors for Enantioenriched β-Hydroxysulfonyl Derivatives.
F. M. Koch, R. Peters, Angew. Chem. Int. Ed. 2007, 46, 2685-2689;
Katalytische enantio- und diastereoselektive Synthese von β-Sultonen: ringgespannte Vorstufen für enantiomerenangereicherte β-Hydroxysulfonylderivate.
Angew. Chem. 2007, 119, 2739–2743.
s12

Macrocyclic Ferrocenyl Bisimidazoline Palladacycle Dimers (FBIPs) as Highly Active and Enantioselective Catalysts for the Aza-Claisen Rearrangement of (Z)-Configured N-para-Methoxyphenyl Trifluoroacetimidates.
S. Jautze, P. Seiler, R. Peters, Angew. Chem. Int. Ed. 2007, 46, 1260–1264;
Makrocyclische Ferrocenyl-Bisimidazolin-Palladacyclus-Dimere als hoch aktive und enantioselektive Katalysatoren für die Aza-Claisen-Umlagerung von Z-konfigurierten N-para-Methoxyphenyltrifluoracetimidaten.
Angew. Chem. 2007, 119, 1282–1286.
s15

Total Syntheses of the Antibacterial Natural Product Abyssomicin C. (highlight article)
R. Peters, D. F. Fischer, Angew. Chem. Int. Ed. 2006, 45, 5736–5739;
Totalsynthesen des antibakteriellen Naturstoffes Abyssomicin C. (highlight article)
Angew. Chem. 2006, 118, 5866–5869.
s16

Practical, Highly Active and Enantioselective Ferrocenyl-Imidazoline Palladacycle Catalysts (FIPs) for the Aza-Claisen Rearrangement of N-para-Methoxyphenyl Trifluoroacetimidates.
M. E. Weiss, D. F. Fischer, Z.-q. Xin, S. Jautze, W. B. Schweizer, R. Peters, Angew. Chem. Int. Ed. 2006, 45, 5694–5699;
Praktikable, hochaktive und enantioselektive Ferrocenyl-Imidazolin-Palladacyclus(FIP)-Katalysatoren für die Aza-Claisen-Umlagerung von N-para-Methoxyphenyltrifluor-acetimidaten.
Angew. Chem. 2006, 118, 5823–5827.
s17
Synthesis and Diastereoselective Ortho-Lithiation / Cyclopalladation of Enantiopure [2-Imidazolyl]-1’,2’,3’,4’,5’-pentamethylferrocenes and -1’,2’,3’,4’,5’-pentaphenylferrocenes.
R. Peters, Z.-q. Xin, D. F. Fischer, W. B. Schweizer, Organometallics 2006, 25, 2917–2920.
s18
Preparation and Diastereoselective ortho-Metalation of Chiral Ferrocenyl Imidazolines: Remarkable Influence of LDA as Metalation Additive.
R. Peters, D. F. Fischer, Org. Lett. 2005, 7, 4137–4140.

s19

F. Hoffmann-La Roche:

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, C. Diolez, A. Rolland, E. Manginot, M. Veyrat, Heterocycles 2007, 72 (Special Issue dedicated to Prof. Yoshito Kishi on the occasion of his 70th birthday), 255-273.
Struktur 20

Scalable Formal Total Syntheses of the Homocamptothecin Derivative and Anti Cancer Agent Diflomotecan via Asymmetric Acetate Aldol Additions to Pyridine Ketone Substrates.
R. Peters, M. Althaus, C. Diolez, A. Rolland, E. Manginot, M. Veyrat, J. Org. Chem. 2006, 71, 5783-5795.
Struktur 21

Process for the manufacture of intermediates in camptothecin production.
R. Peters, PCT Int. Appl. 2006, US 2006189807.

Novel processes for the production of 3-(pyridin-4-yl)-3-hydroxypentanoic acid intermediates.
C. Diolez, E. Manginot, R. Peters, A. Rolland, M. Veyrat, PCT Int. Appl. 2006, WO 2006033011.

Practical Formal Total Synthesis of (rac) and (S)-Camptothecin.
R. Peters, M. Althaus, A.-L. Nagy, Org. Biomol. Chem. 2006, 4, 498-509.
Struktur 22
Efficient Synthesis of a 5-HT2C Receptor Agonist Precursor.
R. Peters, P. Waldmeier, A. Joncour, Org. Proc. Res. Develop. 2005, 9, 508-512.
Struktur 23
Postdoctoral Studies (Harvard University):

Unified Total Synthesis of Pteriatoxins and Their Diastereomers.
F. Matsuura, R. Peters, M. Anada, S. S. Harried, J. Hao, Y. Kishi, J. Am. Chem. Soc. 2006, 128, 7463-7465.
Struktur 24

Ph.D. and Diploma Studies (RWTH Aachen):
SAMP – A Versatile Auxiliary in Asymmetric Synthesis. (review)
A. Job, C. Janeck, W. Bettray, R. Peters, D. Enders, Tetrahedron 2002, 58, 2253-2329.
Struktur 25
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, G. Raabe, J. Runsink, J. W. Bats, Eur. J. Org. Chem. 2000, 3399-3426.
Struktur 26
Enantioselective Synthesis of Planar Chiral ortho-Functionalized Ferrocenylketones.
D. Enders, R. Peters, R. Lochtman, J. Runsink, Eur. J. Org. Chem. 2000, 2839-2850.
Struktur 27
Recovery of Carbonyl Compounds from N,N-Dialkylhydrazones. (account)
D. Enders, L. Wortmann, R. Peters, Acc. Chem. Res. 2000, 33, 157-169.
Struktur 28
Novel Ferrocenyl Ligands with Planar and Central Chirality in Pd-Catalyzed Allylic Substitutions.
D. Enders, R. Peters, J. Runsink, J. W. Bats, Org. Lett. 1999, 1, 1863-1866.

Struktur 29
Asymmetric Synthesis of Novel Ferrocenyl Ligands with Planar and Central Chirality.
D. Enders, R. Peters, R. Lochtman, G. Raabe, Angew. Chem. Int. Ed. 1999, 38, 2421-2423;
Asymmetrische Synthese neuer planar- und zentral-chiraler Ferrocenylliganden.
Angew. Chem. 1999, 111, 2579-2581.
Struktur 30
Enantioselective Synthesis of Planar Chiral ortho-Functionalised Ferrocenylketones.
D. Enders, R. Peters, R. Lochtman, J. Runsink, Synlett 1997, 1462-1464.
Struktur 31