Publikationen

Joachim Podlech: orcid.org/0000-0001-7881-6905; h-Index: 23; Erdös-Zahl: 6

Originalarbeiten - Eigenständig

Bücher, Buchkapitel, Übersichtsartikel und Essays - Eigenständig

Originalarbeiten - Coautorenschaft aus Kooperationen

Originalarbeiten - Postdoktorat

Buchkapitel und Übersichtsartikel - Postdoktorat

Originalarbeiten - Doktorarbeit

Beiträge zu Tagungsbänden, Tagungsberichte, Buchbesprechungen, Nachrufe und Übersetzungen

 

Originalarbeiten–Eigenständig

57 (100). Development of a Robust Protocol for the Determination of Weak Acids’ pKa Values in DMSO
Sebastian T. Jung, Joachim Podlech, J. Org. Chem. 2020, 85, 10951–10957. (doi)

56 (99). Stereoelectronic Effects: Perlin Effects in Thiane-derived Compounds
Sebastian T. Jung, Luis Basche, Tony Reinsperger, Burkhard Luy, Joachim Podlech, Eur. J. Org. Chem. 2020, 2878–2887. (doi)

55 (98). Synthesis of 5,9-Diaza[5]helicenes
Aaron Weiß, Joachim Podlech, Eur. J. Org. Chem. 2019, 66976701. (doi)

54 (94). A New Secondary Metabolite from Alternaria Alternata: Structure Elucidation and Total Synthesis of Altenuic Acid IV
Dominik Kohler, Joachim Podlech, Eur. J. Org. Chem. 2019, 1748-1753. (doi)

53 (92). Stereoelectronic Effects: The γ-Gauche Effect in Sulfoxides
Sebastian Jung, Joachim Podlech, J. Phys. Chem. A 2018, 122, 5764–5772. (doi)

52 (90). Synthesis of cis- and trans-Configured Octahydroperylenes
Dominik Pfaff, Sebastian Bestgen, Joachim Podlech, Eur. J. Org. Chem. 2017, 5666–5670. (doi)

51 (89). Synthesis and acidity of conformationally constrained 1,3-oxathiane S-oxides
Daniel Weingand, Joachim Podlech, Tetrahedron Lett. 2016, 57, 5608–5610. (doi)

50 (88). Stereoelectronic effects in conformations of sulfide, sulfoxide, and sulfone α-carbanions
Bastian D. Süveges, Joachim Podlech, Tetrahedron 2015, 71, 9061–9066. (doi)

49 (87). Conformationally constrained 2-methylidene 1,3-oxathiane S-oxides: synthesis and nucleophilic additions
Daniel Weingand, Claude Kiefer, Joachim Podlech, Tetrahedron 2015, 71, 1261–1268. (doi)

48 (86). Dependence of Stereoelectronic and Charge Effects on pKa Values of 1,3-Dithiane-derived Sulfides, Sulfoxides, and Sulfones. An Experimental and Computational Investigation
Bastian D. Süveges, Joachim Podlech, Eur. J. Org. Chem. 2015, 987–994. (doi)

47 (85). Determination of the Absolute Configuration of Perylene Quinone-derived Mycotoxins by Measurement and Calculation of Electronic Circular Dichroism Spectra and of Specific Rotations
Joachim Podlech, Stefanie C. Fleck, Manfred Metzler, Jochen Bürck, Anne S. Ulrich, Chem. Eur. J. 2014, 11463–11470. (doi)

46 (83). Acid-catalyzed Transacetalization from Glycol to Pinacol Acetals
Yvonne Seeleib, Gregor Nemecek, Dominik Pfaff, Bastian D. Süveges, Joachim Podlech, Synth. Commun. 2014, 44, 2966–2973. (doi)

45 (81). A Lewis Acid-promoted Pinner Reaction
Dominik Pfaff, Gregor Nemecek, Joachim Podlech, Beilstein J. Org. Chem. 2013, 9, 1572–1577. (doi)

44 (79). Structure Elucidation and Total Synthesis of Altenuic Acid III and Studies towards the Total Synthesis of Altenuic Acid II
Gregor Nemecek, Robert Thomas, Helmut Goesmann, Claus Feldmann, Joachim Podlech, Eur. J. Org. Chem. 2013, 6420–6432 (doi).

43 (78). Structure Confirmation of Altertenuol
Robert Thomas, Gregor Nemecek, Joachim Podlech, Nat. Prod. Res. 2013, online erschienen (doi).

42 (77). Synthesis of the Altertoxin III Framework
Oliver Geiseler, Monika Müller, Joachim Podlech, Tetrahedron 2013, 69, 3683–3689. (doi)

41 (76). Conformationally Constrained Oxides of 1,3-Dithiane. Synthesis and NMR-spectroscopic Investigations
Roland Ulshöfer, Tobias Wedel, Bastian Süveges, Joachim Podlech, Eur. J. Org. Chem. 2012, 6867–6877. (doi)

40 (75). A hydrogen chloride-free Pinner reaction promoted by Lewis acids
Dominik Pfaff, Gregor Nemecek, Joachim Podlech, Helv. Chim. Acta 2012, 95, 1851–1856. (doi)

39 (74.) Total synthesis of infectopyrone, aplysiopsenes A–C, ent-aplysiopsene D, phomapyrones A and D, 8,9-dehydroxylarone and nectriapyrone
Oliver Geiseler Joachim Podlech, Tetrahedron 2012, 68, 7280–7287. (doi, Supporting Information)

38 (72). Revision of the Structure and Total Synthesis of Altenuisol
Gregor Nemecek, Judith Cudaj, Joachim Podlech, Eur. J. Org. Chem. 2012, 3863–3870. (doi, Supporting Information)

37 (71). Total Synthesis of Altenusin and Alterlactone
Judith Cudaj, Joachim Podlech, Synlett 2012, 23, 371–374. (doi, Supporting Information)

36 (70). Stereoelectronic Effects in α-Carbanions of Conformationally Constrained Sulfides, Sulfoxides, and Sulfones
Joachim Podlech, J. Phys. Chem. A 2010, 114, 8480–8487. (doi, Supporting Information)

35 (68). γ-Lactam-containing peptidomimetics
Mickael Virlouvet, Joachim Podlech, Tetrahedron 2010, 66, 6174–6180. (doi, Supporting Information)

34 (67). Total Synthesis of graphislactone G
Judith Cudaj, Joachim Podlech, Tetrahedron Lett. 2010, 51, 3092–3094. (doi, Supporting Information)

33 (66). Addition of allylzinc to α-amino acid-derived imines: synthesis of diamino alcohols by hydroboration
Mickael Virlouvet, Helmut Goesmann, Claus Feldmann, Joachim Podlech, Monatsh. Chem. 2010, 141, 177–198. (doi)

32 (65). Stereoelectronic Effects in Vinyl Sulfoxides
Roland Ulshöfer, Joachim Podlech, J. Am. Chem. Soc. 2009, 131, 16618–16619. (doi, Supporting Information)

31 (64). Total Synthesis of Dehydroaltenuene A. Revision of the Structure and Total Synthesis of Dihydroaltenuene B
Martina Altemöller, Joachim Podlech, J. Nat. Prod. 2009, 72, 1288–1290. (doi, Supporting Information)

30 (63). Total Synthesis of Neoaltenuene
Martina Altemöller, Joachim Podlech, Eur. J. Org. Chem. 2009, 2275–2282. (doi, Supporting Information)

29 (62). Total Synthesis of Graphislactones A, C, D, and H, of Ulocladol, and of the Originally Proposed and Revised Structures of Graphislactones E and F
Martina Altemöller, Timo Gehring, Judith Cudaj, Joachim Podlech, Helmut Goesmann, Claus Feldmann, Alexander Rothenberger, Eur. J. Org. Chem. 2009, 2130–2140. (doi, Supporting Information)

28 (59). Synthesis of β,β-diamino acids from α-amino acid-derived β-lactams by ring opening with nucleophiles. Utilization in the synthesis of peptidomimetics
Alexander A. Taubinger, Dieter Fenske, Joachim Podlech, Tetrahedron 2008, 64, 8659–8667. (doi, Supporting Information)

27 (58). Feature Article:
Intramolecular Michael-type Additions to Vinyl Bissulfoxides: Enantioselective Synthesis of Chiral Aldehydes
Timo Gehring, Joachim Podlech, Alexander Rothenberger, Synthesis 2008, 2476–2487. (doi)

26 (55). Nucleophilic Additions to Alkylidenebissulfoxides–Stereoelectronic Effects in Vinylsulfoxides
Tobias Wedel, Timo Gehring, Joachim Podlech, Elena Kordel, Angela Bihlmeier, Wim Klopper, Chem. Eur. J. 2008, 4631–4639. (doi, Supporting Information)

25 (54). Synthesis of β,β'-Diamino Acids from α-Amino Acid-Derived β-Lactams
Alexander A. Taubinger, Dieter Fenske, Joachim Podlech, Synlett 2008, 539–542. (doi)

24 (52). Stereoelectronic Effects in Cyclic Sulfoxides, Sulfones and Sulfilimines: Application of the Perlin Effect to Conformational Analysis
Tobias Wedel, Monika Müller, Joachim Podlech, Helmut Goesmann, Claus Feldmann, Chem. Eur. J. 2007, 13, 4273–4281. (doi, Supporting Information)

23 (49). Alkylidene-[1,3]dithiolane-1,3-dioxides as potent Michael-type acceptors
Tobias Wedel, Joachim Podlech, Synlett 2006, 2043–2046. (doi)

22 (47). Total Synthesis of Altenuene and Isoaltenuene
Martina Altemöller, Joachim Podlech, Dieter Fenske, Eur. J. Org. Chem. 2005, 1678–1684. (doi, Supporting Information)

21 (46). An Exceptionally Simple Homologation of Protected α- to β-Amino Acids in the Presence of Silica Gel
Karen Koch, Joachim Podlech, Synth. Commun. 2005, 35, 2789–2794. (doi)

20 (45). Enolate Addition to 2-Alkylidene[1,3]dithiane-derived Bissulfoxide. A New a2-Akzeptor; Tobias Wedel, Joachim Podlech, Org. Lett. 2005, 7, 4013–4015. (doi - Supporting Information)

19 (43). Total Synthesis of Alternariol
Karen Koch, Joachim Podlech, Erika Pfeiffer, Manfred Metzler, J. Org. Chem. 2005, 70, 3275–3276. (doi)

17 (38). β-Lactam-containing Cyclopeptide Analogs
Thomas C. Maier, Joachim Podlech, Eur. J. Org. Chem. 2004, 4379–4386. (doi - Supporting Information)

16 (37). Utilization of 2-(4-Nitrophenylsulfonyl)ethoxycarbonyl (Nsc) as a Substitute for 9H-Fluoren-9-ylmethoxycarbonyl (Fmoc) in Liquid Phase Chemistry
Thomas C. Maier, Joachim Podlech, Adv. Synth. Catal. 2004, 346, 727–730. (doi)

15 (32). Synthesis of a new turn mimic bearing a β-lactam moiety
Thomas C. Maier, Wolfgang U. Frey, Joachim Podlech, Eur. J. Org. Chem. 2002, 2686–2689. (doi)

14 (31). Indium-induced Addition of Bromomethylacrylates to Phthaloyl-protected Amino Aldehydes
Steffen Steurer, Joachim Podlech, Synthesis 2002, 945–950. (doi)

13 (30). Synthesis of Highly Functionalized Amino Acid and Hydroxy Acid Derivatives from γ-Aminoalkyl-Substituted α-Methylene γ-Butyrolactones; Steffen Steurer, Joachim Podlech, Eur. J. Org. Chem. 2002, 899–916. (doi)

12 (24). Diazoketones as precursors in β-lactam synthesis. New insights into the mechanism of the photochemically induced Staudinger reaction
Michael R. Linder, Wolfgang U. Frey, Joachim Podlech, J. Chem. Soc., Perkin Trans. 1 2001, 2566–2577. (doi - Supporting Information)

11 (23). Synthesis of β-Lactams from Diazoketones and Imines: The Use of Microwave Irradiation
Michael R. Linder, Joachim Podlech, Org. Lett. 2001, 3, 1849–1851. (doi - Supporting Information)

10 (22). Indium-Catalyzed Barbier-Reactions of Amino Aldehydes
Steffen Steurer, Joachim Podlech, Adv. Synth. Catal. 2001, 343, 251–254. (doi

9 (20). A Chiral, Oxidatively Cleavable Auxiliary in Conjugate Additions of Lithium Amides. Preparation of Enantiomerically Pure β-Amino Acid Derivatives
Joachim Podlech, Synth. Commun. 2000, 30, 1779–1786. (doi)

8 (19). Verwendung von Aminosäure-Derivaten in der Synthese neuer Lactame und Lactone (Habilitationsschrift, Universität Stuttgart)
Joachim Podlech, GCA-Verlag: Herdecke, 2000 (ISBN 3-934389-54-6).

7 (16). Synthesis of Peptidomimetics Containing a β-Lactam Moiety Using Peptidic Diazoketones and Imines in a Staudinger Reaction
Michael R. Linder, Joachim Podlech, Org. Lett. 1999, 1, 869–871. (doi)

6 (15). 1,4-Additions to γ-Aminoalkyl-Substituted α-Methylene γ-Butyrolactones: Synthesis of Highly Functionalized Amino Acid Derivatives
Steffen Steurer, Joachim Podlech, Org. Lett. 1999, 1, 481–484. (doi - Supporting Information)

5 (14). Aminoalkyl-Substituted α-Methylene γ-Butyrolactones from α-Amino Acids Using an Indium-Mediated Barbier Allyl Addition
Steffen Steurer, Joachim Podlech, Eur. J. Org. Chem. 1999, 1551–1560. (doi - Supporting Information)

4 (13). Diazoketones - Versatile Starting Materials for the Diastereoselective Synthesis of β-Lactams
Joachim Podlech, Michael R. Linder in Bioorganic Chemistry - Highlights and New Aspects, Hrsg.: Ulf Diederichsen, Thispe K. Lindhorst, Bernd Westermann, Ludger Wessjohann; Wiley-VCH: Weinheim, 1999, 43–47.

3 (12). A Chiral, Oxidatively Cleavable Auxiliary in β-Lactam Synthesis - Double Diastereocontrol with p-Methoxyphenethyl-Substituted Imines; Joachim Podlech, Steffen Steurer, Synthesis 1999, 650–654. (doi)

2 (9). Cycloadditions of Ketenes Generated in The Wolff-Rearrangement. Stereoselective Synthesis of Aminoalkyl-Substituted β-Lactams from α-Amino Acids
Joachim Podlech, Michael R. Linder, J. Org. Chem. 1997, 62, 5873–5883. (doi - Supporting Information)

1 (8). Stereoselective Synthesis of Aminoalkyl-Substituted β-Lactams via Cycloaddition of Ketenes Generated from α-Amino Acids
Joachim Podlech, Synlett 1996, 582–584. (doi)

Bücher, Buchkapitel, Übersichtsartikel und Essays–Eigenständig

28 (97). Phosphorus Analogues of Guanidine (Update 2019)
Joachim Podlech in Science of Synthesis Knowledge Updates 2019/1, Hrsg.: M. C. Bagley, K. Banert, N. Krause, M. Yus; Georg Thieme Verlag: Stuttgart, New York, 2019, 1, 433–449.

27 (96). Guanidine Derivatives (Update 2019)
Joachim Podlech in Science of Synthesis Knowledge Updates 2019/1, Hrsg.: M. C. Bagley, K. Banert, N. Krause, M. Yus; Georg Thieme Verlag: Stuttgart, New York, 2019, 1, 387–431.

26 (95). Phosphorus Analogues of Guanidine (Update 2019)
Joachim Podlech in Science of Synthesis Knowledge Updates 2019/1, Hrsg.: M. C. Bagley, K. Banert, N. Krause, M. Yus; Georg Thieme Verlag: Stuttgart, New York, 2019, 1, 433–449.

25 (93). Acyclic and Cyclic Carbamic Acids and Esters, and Their Sulfur, Selenium, Tellurium, and Phosphorus Analogues (Update 2018)
Joachim Podlech in Science of Synthesis Knowledge Updates 2018/4, Hrsg.: K. Banert, P. A. Clarke, J. Drabowicz, M. Oestreich; Georg Thieme Verlag: Stuttgart, New York, 2018, 4, 113–207.

24 (84). Siegfried Hünig, Gottfried Märkl, Jürgen Sauer, Peter Kreitmeier, Alfons Ledermann, Arbeitsmethoden in der organischen Chemie, 3. Aufl., Hrsg.: Joachim Podlech; Lehmann Media: Berlin, 2014.

23 (80). Cyanogen Halides, Cyanates and Their Sulfur, Selenium, and Tellurium Analogues, Sulfinyl and Sulfonyl Cyanides, Cyanamides, and Phosphaalkynes (Update 2013)
Joachim Podlech in Science of Synthesis: Knowledge Updates 2013/2, Hrsg.: K. Banert, J. Drabowicz, M. Oestreich, B. J. Plietker, C. Ramsden, E. Schaumann, B. M. Stoltz, S. M. Weinreb; Georg Thieme Verlag: Stuttgart, New York, 2013, 2, 265–287.

22 (69). „Wünscht lieber, dass ich krank sei ...“–Der Komponist, Chemiker und Mediziner Alexander Borodin
Joachim Podlech, Angew. Chem. 2010, 122, 6636–6642. (doi, Supporting Information)

„Try and fall sick …“–The Composer, Chemist and Surgeon Aleksandr Borodin
Joachim Podlech, Angew. Chem. Int. Ed. 2010, 49. 6490 - 6495. (doi, Supporting Information)

21 (51). Synthesis of Aldehydes by Oxidation
Joachim Podlech in Science of Synthesis: Houben-Weyl Methods of Molecular Transformation - Category 4: Compounds with Two Carbon-Heteroatom Bonds ,Vol. 25: Aldehydes and Heteroatom Analogues, Hrsg.: Reinhard Brückner; Georg Thieme Verlag: Stuttgart, 2007, 25–56.

20 (50). Synthesis of Aldehydes by Oxidative Cleavage
Joachim Podlech in Science of Synthesis: Houben-Weyl Methods of Molecular Transformation - Category 4: Compounds with Two Carbon-Heteroatom Bonds ,Vol. 25: Aldehydes and Heteroatom Analogues, Hrsg.: Reinhard Brückner; Georg Thieme Verlag: Stuttgart, 2007, 17–23.

19 (44). Fortschritte bei der asymmetrischen Autokatalyse nach Soai
Joachim Podlech, Timo Gehring Angew. Chem. 2005, 117, 5922–5924. (doi)

New Aspects of Soai's Asymmetric Autocatalysis
Joachim Podlech, Timo Gehring Angew. Chem. Int. Ed. 2005, 44, 5776–5777. (doi)

18 (42). Preparation of Enantiopure β-Amino Acids by Homologation of α-Amino Acids
Joachim Podlech in Enantioselective Synthesis of β-Amino Acids, Hrsg.: Eusebio Juaristi, Vadim A. Soloshonok; John Wiley & Sons: Hoboken, 2005, 93–106.

17 (41). Introduction of the Cyanide Group by Addition to Alkenes
Joachim Podlech in Science of Synthesis: Houben-Weyl Methods of Molecular Transformation - Category 3: Compounds with Four and Three Carbon-Heteroatom Bonds, Vol. 19: Three Carbon-Heteroatom Bonds: Nitriles, Isonitriles, and Their Derivatives, Hrsg.: Shun-ichi Murahashi; Georg Thieme Verlag: Stuttgart, 2004, 333–344.

16 (40). Introduction of the Cyanide Group by Addition to Alkynes
Joachim Podlech in Science of Synthesis: Houben-Weyl Methods of Molecular Transformation - Category 3: Compounds with Four and Three Carbon-Heteroatom Bonds, Vol. 19: Three Carbon-Heteroatom Bonds: Nitriles, Isonitriles, and Their Derivatives, Hrsg.: Shun-ichi Murahashi; Georg Thieme Verlag: Stuttgart, 2004, 325–331.

15 (39). Introduction of the Cyanide Group by Conjugate Addition
Joachim Podlech in Science of Synthesis: Houben-Weyl Methods of Molecular Transformation - Category 3: Compounds with Four and Three Carbon-Heteroatom Bonds, Vol. 19: Three Carbon-Heteroatom Bonds: Nitriles, Isonitriles, and Their Derivatives, Hrsg.: Shun-ichi Murahashi; Georg Thieme Verlag: Stuttgart, 2004, 311–324.

14 (36). Indium in Organic Synthesis
Joachim Podlech, Thomas C. Maier, Synthesis 2003, 633–655. (doi)

13 (35). Metalated Tin Compounds (Sn-M, except M = As, Sb, Bi, Si, Ge)
Joachim Podlech in Science of Synthesis: Houben-Weyl Methods of Molecular Transformation - Category 1: Organometallics, Vol. 5: Compounds of Group 14 (Ge, Sn, Pb), Hrsg.: Mark G. Moloney; Georg Thieme Verlag: Stuttgart, 2003, 285–297.

12 (34). Distannenes, Distannanes (Sn=Sn, Sn-Sn)
Joachim Podlech in Science of Synthesis: Houben-Weyl Methods of Molecular Transformation - Category 1: Organometallics, Vol. 5: Compounds of Group 14 (Ge, Sn, Pb), Hrsg.: Mark G. Moloney; Georg Thieme Verlag: Stuttgart, 2003, 273–283.

11 (33). (S)-3-(tert-Butoxycarbonylamino)-4-phenylbutanoic Acid
Michael R. Linder, Steffen Steurer, Joachim Podlech, Org. Synth. 2002, 79, 154–164. (Überprüft von Frédéric Berst, Andrew B. Holmes.) (Im Netz suchbar)

10 (29). Peptide Bond Formation - Carbonyldiimidazole
Joachim Podlech in Houben-Weyl, Methods of Organic Chemistry, Additional and Supplementary Volume E22a to the 4th Edition, Synthesis of Peptides and Peptidomimetics, Hrsg.: Murray Goodman, Arthur Felix, Luis Moroder, Claudio Toniolo; Georg Thieme Verlag: Stuttgart, 2001, 534–537.

9 (28). Peptide Bond Formation - Carbodiimides
Joachim Podlech in Houben-Weyl, Methods of Organic Chemistry, Additional and Supplementary Volume E22a to the 4th Edition, Synthesis of Peptides and Peptidomimetics, Hrsg.: Murray Goodman, Arthur Felix, Luis Moroder, Claudio Toniolo; Georg Thieme Verlag: Stuttgart, 2001, 517–533.

8 (27). Protection of Functional Groups - ω-Amino Group
Joachim Podlech, Hans-Jürgen Musiol, Elisabeth Lohof, Luis Moroder in Houben-Weyl, Methods of Organic Chemistry, Additional and Supplementary Volume E22a to the 4th Edition, Synthesis of Peptides and Peptidomimetics, Hrsg.: Murray Goodman, Arthur Felix, Luis Moroder, Claudio Toniolo; Georg Thieme Verlag: Stuttgart, 2001, 166–192.

7 (26). Protection of Functional Groups - α-Amino Group
Joachim Podlech, Marion Gurrath, Gerhard Müller, Elisabeth Lohof in Houben-Weyl, Methods of Organic Chemistry, Additional and Supplementary Volume E22a to the 4th Edition, Synthesis of Peptides and Peptidomimetics, Hrsg.: Murray Goodman, Arthur Felix, Luis Moroder, Claudio Toniolo; Georg Thieme Verlag: Stuttgart, 2001, 41–165.

6 (25). Origin of Organic Molecules and Biomolecular Homochirality
Joachim Podlech, Cell. Mol. Life Sci. 2001, 58, 44–60. (doi)

5 (21). Diazoketones as Precursors in β-Lactam Synthesis
Joachim Podlech, Michael R. Linder, Thomas C. Maier, Targets Heterocycl. Syst. 2000, 4, 269–291.

Joachim Podlech, Michael R. Linder, Thomas C. Maier, in Targets in Heterocyclic Systems - Chemistry and Properties, Bd. 4, Hrsg.: Orazio A. Attanasi, Domenico Spinelli; Società Chimica Italiana: Rom, 2000, 269–291.

4 (18). Elimination of Fluorine to Form C-N-Bonds
Joachim Podlech in Houben-Weyl, Methods of Organic Chemistry, Additional and Supplementary Volume E10b / Part 2 to the 4th Edition, Organo-Fluorine Compounds, Hrsg.: Bernd Baasner, Hermann Hagemann, J. Colin Tatlow; Georg Thieme Verlag: Stuttgart, 1999, 449–464.

3 (17). Neue Einblicke in den Ursprung der Homochiralität biologisch relevanter Moleküle - Grundstoffe des Lebens aus dem All?
Joachim Podlech, Angew. Chem. 1999, 111, 501–502. (doi)

New Insight in the Source of Biomolecular Homochirality: An Extraterrestrial Origin for the Molecules of Life?
Joachim Podlech, Angew. Chem. Int. Ed. 1999, 38, 477–478. (doi)

2 (11). Trimethylsilyldiazomethane (TMS-CHN2) and Lithiated Trimethylsilyldiazomethane; Versatile Substitutes for Diazomethane
Joachim Podlech, J. prakt. Chem. 1998, 340, 679–682. (doi)

1 (10). Dirhodium(II) Tetrakis(Methyl Pyrrolidone-5-carboxylate) [Rh2(5R-mepy)4 and Rh2(5S-mepy)4] and Related Chiral Rhodium Catalysts
Joachim Podlech, J. prakt. Chem. 1998, 340, 479–482. (doi)

Originalarbeiten–Coautorenschaft aus Kooperationen

9 (101). DNA Reactivity of Altertoxin II: Identification of Two Covalent Guanine Adducts Formed under Cell-free Conditions
Sebastian T. Soukup, Stefanie C. Fleck, Erika Pfeiffer, Joachim Podlech, Sabine E. Kulling, Manfred Metzler, Toxicol. Lett.. 2020, 331, 75–81. (doi)

8 (91). Tracking emerging mycotoxins in food: Development of an LC-MS/MS method for free and modified Alternaria toxins
Hannes Puntscher, Mary-Liis Kütt, Philipp Skrinjar, Hannes Mikula, Joachim Podlech, Johannes Fröhlich, Doris Marko, Benedikt Warth, Anal. Bioanal. Chem. 2018, 410, 4481 - 4494 (doi).

7 (73). Identification of a polyketide synthase required for alternariol (AOH) and alternariol-9-methyl ether (AME) formation in Alternaria alternata
Debjani Saha, Ramona Fetzner, Britta Burkhardt, Joachim Podlech, Manfred Metzler, Ha Dang, Christopher Lawrence, Reinhard Fischer, PLoS One 2012, 7, e40564. (doi)

6 (61). Glucuronidation of the mycotoxins alternariol and alternariol-9-methyl ether in vitro: chemical structures of glucuronides and activities of human UDP-glucuronosyltransferase isoforms
E. Pfeiffer, C. Schmit, B. Burkhardt, M. Altemöller, J. Podlech, M. Metzler, Mycotoxin Res. 2009, 25, 3–10. (doi)

5 (60). Activities of human recombinant cytochrome P450 isoforms and human hepatic microsomes for the hydroxylation of Alternaria toxins
E. Pfeiffer, B. Burkhardt, M. Altemöller, J. Podlech, M. Metzler, Mycotoxin Res. 2008, 24, 117–123. (doi)

4 (57). Oxidative in vitro metabolism of the Alternaria toxins altenuene and isoaltenuene
Erika Pfeiffer, Carina Herrmann, Martina Altemöller, Joachim Podlech, Manfred Metzler, Mol. Nutr. Food Res. 2009, 53, 452–459. (doi)

3 (56). Alternariol acts as a topoisomerase poison, preferentially affecting the IIα isoform
Markus Fehr, Gudrun Pahlke, Jessica Fritz, Fritz Boege, Martina Altemöller, Joachim Podlech, Doris Marko, 2009, 53, 441–451. (doi)

2 (53). Novel oxidative in vitro metabolites of the mycotoxins alternariol and alternariol methyl ether
Erika Pfeiffer, Nils H. Schebb, Joachim Podlech, Manfred Metzler, Mol. Nutr. Food Res. 2007, 51, 307–316. (doi)

1 (48). Mutagenicity of the Mycotoxin Alternariol in Cultured Mammalian Cells
Eva-Maria Brugger, Jörg Wagner, David M. Schumacher, Karen Koch, Joachim Podlech, Manfred Metzler, Leane Lehmann, Toxicol. Lett. 2006, 164, 221–230. (doi)

Originalarbeiten–Postdoktorat

4 (7). Selective Acylations of Multifunctional Nucleophiles, Including Carbohydrates and Nucleosides, with Intermediates Generated by Wolff Rearrangement of Amino Acid Derived Diazo Ketones: Preparation of β-Amino Acid Derivatives
Christel Guibourdenche, Joachim Podlech, Dieter Seebach, Liebigs Ann. 1996, 1121–1129. (doi)

3 (5). Azetidin-3-ones from (S)-β-Amino Acids and Their Reactions with Nucleophiles: Preparation of Some Azetidine-Containing Amino-Alcohol and Amino-Acid Derivatives
Joachim Podlech, Dieter Seebach, Helv. Chim. Acta 1995, 78, 1238–1246. (doi)

2 (4). On the Preparation of β-Amino Acids from α-Amino Acids Using the Arndt-Eistert Reaction: Scope, Limitations and Stereoselectivity. Application to Carbohydrate Peptidation. Stereoselective α-Alkylations of Some β-Amino Acids
Joachim Podlech, Dieter Seebach, Liebigs Ann. 1995, 1217–1228. (doi)

1 (3). Die Arndt-Eistert-Reaktion in der Peptidchemie: ein einfacher Zugang zu Homopeptiden
Joachim Podlech, Dieter Seebach, Angew. Chem. 1995, 107, 507–509.(doi)

The Arndt-Eistert Reaction in Peptide Chemistry: A Facile Access to Homopeptides
Joachim Podlech, Dieter Seebach, Angew. Chem. Int. Ed. Engl. 1995, 34, 471–472. (doi)

Buchkapitel und Übersichtsartikel–Postdoktorat

1 (6). (R)-Methyl 2-t-Butyl-3(2H)-oxazole-carboxylate
J. Podlech, D. Seebach in Encyclopedia of Reagents for Organic Synthesis, Hrsg.: Leo A. Paquette; John Wiley & Sons: Chichester, 1995, Bd. 5, S. 3452–3453.

Originalarbeiten–Doktorarbeit

2 (2). Reaction of 1-(Halomethyl)bicyclo[1.1.1]pentanes with Strong Bases: Evidence for a Carbene-Bridgehead Olefin-Carbene Rearrangement
Uwe Bunz, Walter Herpich, Joachim Podlech, Kurt Polborn, Angelika Pratzel, David S. Stephenson, Günter Szeimies, J. Am. Chem. Soc. 1994, 116, 7637–7641. (doi - supporting information)

1 (1). Tetracyclo[3.2.0.02,7.04,6]hept-1-ene: Formation and Trapping of 1,2-Dehydroquadricyclane. Ab Initio Calculations on Dehydroquadricyclanes
Joachim Podlech, Kurt Polborn, Günter Szeimies, J. Org. Chem. 1993, 58, 4113–4117. (doi)

Beiträge zu Tagungsbänden, Tagungsberichte, Buchbesprechungenn Nachrufe und Übersetzungen

14. William H. Brown, Thomas Poon, Einführung in die Organische Chemie, Wiley-VCH: Weinheim, 2020; übersetzt von Joachim Podlech.

13. Felix Lee, William H. Brown, Thomas Poon, Einführung in die Organische Chemie: Arbeitsbuch, Wiley-VCH: Weinheim, 2020; übersetzt von Joachim Podlech.

12. Buchbesprechung: Stereoelectronic Effects ‒ A Bridge between Structure and Reactivity, Igor V. Alabugin, John Wiley and Sons: Hoboken, 2016;
Joachim Podlech, Angew. Chem. 2017, 129, 3183. (doi)
Joachim Podlech, Angew. Chem. Int. Ed. 2017, 56, 3137. (doi)

11. Buchbesprechung: Efficiently Studying Organic Chemistry, Eberhard Breitmaier, Thieme: Stuttgart, 2015;
Joachim Podlech, Synthesis 2015, 47, 1960. (doi)

10. Ian Fleming, "Molekülorbitale und Reaktionen organischer Verbindungen"; Wiley-VCH: Weinheim, 2012; übersetzt von Joachim Podlech.

9. 150 Jahre Weltkongress Chemie
Joachim Podlech, Nachr. Chem. 2010, 58, 1173. (doi)

8. 150th Anniversary Weltkongress Chemie
Joachim Podlech, http://dx.doi.org/10.1002/chemv.201000026

7. "150th Anniversary Weltkongress Chemie": Fortschritt und Herausforderungen der Chemie
Joachim Podlech, http://www.kit.edu/besuchen/2938.php

6. Leopold Horner (1911–2005)–Ehrendoktor der Universität Karlsruhe (TH) im Alter von 94 Jahren verstorben
Joachim Podlech, (pdf).

5. Buchbesprechung: Peptides: Chemistry and Biology, Norbert Sewald, Hans-Dieter Jakubke, Wiley-VCH, Weinheim, 2002
Joachim Podlech, Nachr. Chem. 2003, 51, 961.

4. Neue Synthesen von β-Lactamen
Joachim Podlech, Michael R. Linder, Thomas C. Maier, Chemie in Stuttgart–Sonderausgabe Bunsentagung 2001 Mai 2001, 64–66.

3. Doktoranden stellen ihre Ergebnisse vor
Joachim Podlech, Jörg Pietruszka, Stuttgarter unikurier 2000, Nr. 84 / 85, 97.

2. Tag der Organischen Chemie in Stuttgart
Joachim Podlech, Jörg Pietruszka, Nachr. Chem. 2000, 48, 219.

1. Diazoketone als Ausgangsverbindungen in diastereoselektiven β-Lactam-Synthesen
Joachim Podlech, Michael R. Linder in 6. Nachwuchswissenschaftler-Symposium Bioorganische Chemie [22.–24. September 1997, Paderborn], Hrsg.: Ludger A. Wessjohann, Thispe K. Lindhorst, Bernd Westermann, Ulf Diedrichsen; Prosciencia Verlagsbuchhandel Ulrich C. Philipp: Köln, 1997.