Dr. Michael R. Linder

  • Promotion in Stuttgart


1) 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)

2) 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) 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)

4) 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.

5) 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)

6) 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)

7) (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)