AK-Thiem

Prof. Dr.
Joachim Thiem

University of Hamburg
Department of Chemistry Faculty of Sciences
Martin-Luther-King-Platz 6
D-20146 Hamburg
Ph: +49 40 42838 - 4241
Fax: +49 40 42838 - 4325
thiem@chemie.uni-hamburg.de

Recent Publications (2009-2011)

409. Aziridine ring opening as regio- and stereoselective access to O-glycosyl amino acids and their transformation into O-glycopeptide mimetics
A. Schaefer, D. Henkensmeier, L. Kroeger, J. Thiem
Tetrahedron: Asymmetry 20, 902-909 (2009)

410.
Comparative solution and solid-phase glycosylations toward a disaccharide library
K. Agoston, L. Kroeger, A. Agoston, G. Dekany, J. Thiem
Carbohydr. Res. 344, 1428-1433 (2009)

411. En route to deoxygenated N-acetyllactosamine analogues employing uridyl and galactosyl transferases
D. Lazarevic, H. Streicher, J. Thiem
Carbohydr. Res. 344, 12, 1449-1452 (2009)

412. Benzyl Ethers as Nucleophiles: From Hydroxy Cyclooctanes Towards Bridged C-Furanosides
S. Jürs, J. Thiem
J. Carbohydr. Chem. 28, 293-297 (2009)


413. Synthesis of novel gluco- and galacto-functionalized platinum complexes
J. Möker, J. Thiem
Eur. J. Org. Chem. 28, 4842-4647 (2009)

414. Solid-Phase Random Glycosylation
K. Agoston, L. Kroeger, A. Agoston, G. Dekany, J. Thiem
J. Comb. Chem. 11, 813-819 (2009)

415. Glycostructures in Biological Systems-Synthesis and Function
J. Thiem, T. Braulke
Eur. J. Cell. Biol. 89, 1 (2010)

416. Enzymatic Glycosylation and Inhibitor Design. Synthesis and Formation of GlycoSAMs
for Simulation and Recognition
A. M. Scheppokat, A. Gerber, A. Schroven, S. Meinke, S. Kopitzki, E. Beketow,
J. Thimm, J. Thiem
Eur. J. Cell. Biol. 89, 39-52 (2010)

417. A Highly Versatile Octasubstituted Phthalocyanine Scaffold for ex post Chemical
Diversification
H. J. Berthold, T. Schotten, F. Hoffmann, J. Thiem
Synthesis 5, 741-748 (2010)

418. Synthesis of Novel Amino-bridged Oligosaccharide Mimetics
J. Neumann, J. Thiem
Eur. J. Org. Chem. 900-908 (2010)

419. Chemical synthesis using enzymatically generated building units for construction of the human milk pentasaccharides sialyllacto-N-tetraose and sialyllacto-N-neotetraose epimer
D. Schmidt, J. Thiem
Beilstein J. Org. Chem. 6, No. 18 (2010)

420. Formation of Homooligosaccharides Using Base Promoted Glycosylation of Unprotected Glycosyl Fluorides
A. Steinmann*; J. Thimm*, M. Matwiejuk, J. Thiem
Macromolecules 43, 3606-3612 (2010)

421. Ex Post Glycoconjugation of Phthalocyanines
H. J. Berthold, S. Franke, J. Thiem, T. Schotten
J. Org. Chem. 75, 3859-3862 (2010)

422. Synthesis of Benzaldehyde Functionalized Glycans: Novel Approach Towards Glyco- SAMs as Tools for Surface Plasmon Resonance Studies
S. Kopitzki, K. J. Jensen, J. Thiem
Chem. Eur. J. 16, 7017-7029 (2010)

423. Spiro-annelated Zn-phthalocyanine a novel building block for molecular architecture
H.J. Berthold, J. Thiem, A. Zaliani, T. Schotten  Synthesis, 3569-3575 (2010)

424. Synthesis of Carbohydrate-based Azamacrocycles by Richman-Atkins Cyclisation
A. Rathjens, J. Thiem  Compt. Rend. Chim. 14, 286-300 (2011)

425. Transformations of Chromanol and Tocopherol and Synthesis of Ascorbate Conjugates
M. Lahmann, J. Thiem  Tetrahedron 67, 1654-1664 (2011)

426. Synthesis of Saccharide-Derived Functional Polymers
J. Thimm, J. Thiem  in "Green Polymerization Methods" Eds.: R. T. Mathers, M. A. R. Meier, Wiley-VCH, Weinheim, 2011, p. 221-234

427. Sialic Acid C-Glycosides with Aromatic Residues: Investigating Enzyme Binding and
Inhibition of Tripanosoma cruzi Trans-sialidase
S. Meinke, A. Schroven, J. Thiem
Org. Biomol. Chem. 9, 4487-44497 (2011)

428. En route to sugar-alkaloid conjugates
C.-E. Sowa, J. Thiem
Carbohydr. Res. 346, 1546 - 1550 (2011)

429.    Defining Oxyanion Reactivities in Base-promoted Glycosylation
M. Matwiejuk, J. Thiem
Chem.Commun. 47, 8379 - 8381 (2011)

430. Highly efficient synthesis of ketoheptoses
D.Waschke, J.Thimm, J.Thiem
Org. Lett., 13, 3628-3631 (2011)

431. Novel Method for Regioselective Glycosylation Employing Saccharide Oxyanions
M. Matwiejuk, J. Thiem
Eur. J. Org. Chem. 5860-5878 (2011)  

University of Hamburg | Chemistry in Hamburg | Institute of Organic Chemistry | AK Thiem Group