2010-2006

139   R. Pratap, U. Kazmaier, "Synthesis of 1-Stannylated and Iodinated 1-Chloroalkenes as Versatile Synthetic Intermediates", Synlett 2010, 3073–3077.

138   U. Kazmaier, A. Persch, "A straightforward approach towards 5-substituted thiazolylpeptides via thio-Ugi-reaction", Org. Biomol. Chem. 2010, 8, 5442-5447.

137   A. Bayer, U. Kazmaier, "Highly Regioselective Ruthenium-catalyzed Allylic Alkylations of Chelated Enolates", Org. Lett. 2010, 12, 4960–4963.

136   Y. Chai, D. Pistorius, A. Ullrich, K. J. Weissman, U. Kazmaier, R. Müller, "Discovery of 23 Novel Natural Tubulysins from Angiococcus disciformis An d48 and Cystobacter SBCb004", Chem. Biol. 2010, 17, 296–309.

135   S. Samsoniya, M. Trapaidze, N. Nikoleishvili, K. Japaridze, J. Maisuradze, U. Kazmaier, "Dipyrroloquinoxaline. 1. Synthesis of a new bisspiropyrane system on the basis of benzo[e]­pyrrolo[3,2-g]-indole", Chem. Heterocycl. Comp. 2010, 1020–1022.

134   S. Samsoniya, M. Trapaidze, N. Nikoleishvili, K. Japaridze, J. Maisuradze, U. Kazmaier, "Bisindoles. 42. Synthesis of a new bisspiropyrane system on the basis of indolo[4,5-e]-indole", Chem. Heterocycl. Comp. 2010, 1016–1019.

133   A. Z. Kalatozishvili, N. L. Targamadze, I. S. Chikvaidze, S. A. Samsoniya, A. O. Wesquet, U. Kazmaier, "A Straightforward Approach towards the Synthesis of New Bis-Pyridazino-indoles", Chem. Heterocycl. Comp. 2010, 608–612.

132   S. Rachid, O. Reverman, C. Dauth, U. Kazmaier, R. Müller, "Characterization of a Novel Type of Oxidative Decarboxylase involved in the Biosynthesis of the Styryl Moiety of Chondrochloren from an acylated Tyrosine", J. Biol. Chem. 2010, 285, 12482–12489.

131   B. V. Lakshmi, U. Kazmaier, "A straightforward approach towards substituted Morita-Baylis-Hillman (MBH) products via hydrostannation of acetylenic ketones", Synlett 2010, 407-410.

130   S. Thies, U. Kazmaier, "Vinylepoxides as Versatile Substrates for Allylations of Amino Acids and Peptides", Synlett 2010, 137-141.

129   D. Gawas, U. Kazmaier, "Diastereotopos-differentiating allylic alkylation as key step in natural product synthesis", Org. Biomol. Chem. 2010, 8, 457–462.

128   A. Ullrich, J. Herrmann, R. Müller, U. Kazmaier, "Synthesis and biological evaluation of pretubulysin and derivatives", Eur. J. Org. Chem. 2009, 6367-6378.

127   U. Kazmaier, C. Schmidt, "Synthesis of Furanoid Amino Acids via a Domino Michael-/ Aldol-Addition/Cyclization-Approach", Synlett 2009, 2625-2628.

126   C. Bukovec, U. Kazmaier, "A Straightforward Protocol for One-pot Allylic Aminations/Stille Couplings", Org. Lett. 2009, 11, 3518-3521.

125   U. Kazmaier, "Erdalkalimetall-katalysierte direkte Michael-, Aldol- und Mannich-Additionen", Angew. Chem. 2009, 121, 5902-5904; Angew. Chem. Int. Ed. 2009, 47, 5790-5792.

124   U. Kazmaier, C. Schmidt, "Synthesis of Highly Functionalized Proline Derivatives via a One-Pot Michael-/SN’-Addition/Cyclization-Approach", Synthesis 2009, 2435-2439.

123   A. O. Wesquet, U. Kazmaier, "Improved Protocols for Molybdenum- und Tungsten-catalyzed Hydrostannations", Adv. Synth. Catal. 2009, 1395-1404.

122   A. Ullrich, Y. Chai, D. Pistorius, Y. A. Elnakady, J. E. Herrmann, K. J. Weissman, U. Kazmaier, and R. Müller, "Pretubulysin, a potent and chemically-accessible tubulysin precursor from Angiococcus disciformis", Angew. Chem. 2009, 121, 4486-4489; Angew. Chem. Int. Ed. 2009, 47, 4422-4425.

121   M. Bauer, U. Kazmaier, "Straightforward syntheses of chiral hydroxy isocyanides", Eur. J. Org. Chem. 2009, 2360-2366.

120   C. Quirin, U. Kazmaier, "Stereoselective Synthesis of β-Branched Phenylalanine-Derivatives via Chelate-Claisen Rearrangement", Synthesis 2009, 1725-1731.

119   U. Kazmaier, C. Schmidt, "Synthesis of Highly Functionalized Proline Derivatives via a One-pot Michael-/Aldol-Addition/Cyclization-Approach", Synlett 2009, 1136-1140.

118   H. Lin, U. Kazmaier, "Molybdenum-Catalyzed α-Hydrostannations of Propargyl Amines as Key Step for the Synthesis of N-Heterocycles", Eur. J. Org. Chem. 2009, 1221-1227.

117   D. Gawas, U. Kazmaier, "Highly Diastereoselective anti-Aldol Reactions of Glycolate Titanium Enolates", J. Org. Chem. 2009, 74, 1788-1790.

116   C. Quirin, U. Kazmaier, "Synthesis of Chlamydocin via Chelate-Claisen Rearrangement", Eur. J. Org. Chem. 2009, 371-377.

115   K. Krämer, J. Deska, C. Hebach, U. Kazmaier, "A straightforward approach towards glycoamino acids and glycopeptides via Pd-catalysed allylic alkylation", Org. Biomol. Chem. 2009, 7, 103-110.

114   F. Maurer, M. Bauer, S. M. Hoffmann, U. Kazmaier, "Hydroxyalkyl Thiazolines, a new Class of Highly Efficient Ligands for Carbonyl Additions", Synlett 2008, 3203-3207.

113   C. Schmidt, U. Kazmaier, "Synthesis of highly substituted pyroglutamates via a domino Michael addition / Claisen rearrangement / lactamization approach", Org. Biomol Chem. 2008, 6, 4654-4648.

112   N. S. Samsonia, A. Z. Kalatozishvili, N. L. Targamadze, I. S. Chikvaidze, S. A. Samsoniya, A. O. Wesquet, U. Kazmaier, "A Straightforward Approach towards the Synthesis of New Bis-Pyridazino-indoles", J. Heterocycl. Chem. 2008, eingereicht.

111   S. A. Samsoniya, M. Trapaidze, N. Nikoleishvili, A. O. Wesquet, U. Kazmaier, "Pyrroloindoles. Synthesis of a new spirocyclic system based on benzo[e]pyrrolo[3,2-g]indole", Chem. Heterocycl. Comp. 2008, 1260-1262.

110   D. S. Zurabishvili, M. O. Lomidze, S. A. Samosoniya, A. O. Wesquet, U. Kazmaier, "The synthesis and transformation of some 5(6)-1-adamantyl benzimidazole", Chem. Heterocycl. Comp. 2008, 44, 941-950.

109   S. Basak, U. Kazmaier, "Palladium-catalyzed Dienylations of Chelated Enolates", Eur. J. Org. Chem. 2008, 4169-4177.

108   D. Stolz, U. Kazmaier, "Rhodium-Catalyzed Allylic Alkylations as Key Steps in the Synthesis of Cyclic α-Alkylated Amino Acids", Synthesis 2008, 2288-2292.

107   N. Jena, U. Kazmaier, "Synthesis of stannylated allyl and vinyl phosphonates via molybdenum catalyzed hydrostannations", Eur. J. Org. Chem. 2008, 3852-3858.

106   N. L. Targamadze, N. S. Samsonia, D. O. Kadjrishvili, I. S. Chikvaidze, S. A. Samsoniya, A. Wesquet, U. Kazmaier, "Some new transformations of pyrroloindole. Synthesis of new derivatives of 1H,6H-pyrrolo[2,3-]indole", Proceedings of the Georgian National Academy of Sciences 2008, 34, 35-39.

105   J. Deska, U. Kazmaier, "Peptide backbone modifications", Curr. Org. Chem. 2008, 355-385.

104   A. O. Wesquet, U. Kazmaier, "Distannylierung und Silastannylierung in situ generierter Allene", Angew. Chem. 2008, 120, 3092-3096; Angew. Chem. Int. Ed. 2008, 47, 3050-3053.

103   S. Basak, U. Kazmaier, "Allylations of Chelated Enolates using Dienyl Substrates", Org. Lett. 2008, 10, 501-504.

102   C. Schmidt, U. Kazmaier, "Efficient Stereoselective Syntheses of Constrained Glutamates via Michael Induced Ring Closing Reactions", Eur. J. Org. Chem. 2008, 887-894.

101   U. Kazmaier, D. Stolz, K. Krämer, F. Zumpe, "Influences on the Regioselectivity of Palladium-catalyzed Allylic Alkylations", Chem. Eur. J. 2008, 14, 1322-1329.

100   U. Kazmaier, S. Hähn, T. D. Weiss, W. F. Maier, R. Kautenburger, "Palladium-doped Mixed Oxides as "Slow Release" Catalysts for Suzuki Couplings", Synlett 2007, 2579-2583.

99   J. Deska, U. Kazmaier, "Highly Stereoselective Peptide Modifications via Palladium Catalyzed Allylic Alkylations of Chelated Peptide Enolates", Chem. Eur. J. 2007, 13, 6204-6211.

98   J. Deska, U. Kazmaier, "Stereoselektive Synthese und Umsetzung stannylierter Peptide", Angew. Chem. 2007, 119, 4654-4657; Angew. Chem. Int. Ed. 2007, 46, 4570-4573.

97   H. Lin, U. Kazmaier, "Regioselective Mo-catalyzed hydrostannations as key steps in the synthesis of functionalized amino alcohols and heterocycles", Eur. J. Org. Chem. 2007, 2839-2843.

96   U. Kazmaier, S. Dörrenbächer, A. Wesquet, S. Lucas, M. Kummeter, "Molybdenum-catalyzed Synthesis of Stannylated Allylic Alcohol Derivatives and their Synthetic Applications", Synthesis 2007, 320-326.

95   D. Stolz, U. Kazmaier, R. Pick, "Aromatic Nitro Groups and their Reactions with Chelated Ester Enolates", Synthesis 2006, 3341-3347.

94   U. Kazmaier, K. Krämer, "Isomerisierungsfreie Allylische Alkylierungen via terminale π-Allyl-Palladium-Komplexe", J. Org. Chem. 2006, 71, 8950-8953.

93   D. Stolz, R. Pick, U. Kazmaier, "Chelated Ester Enolates as versatile Nucleophiles for direct nucleophilic attack on aromatic nitro groups", Synlett 2006, 1616-1618.

92   U. Kazmaier, J. Deska, A. Watzke, "Stereoselektive Palladium-katalysierte Allylierung von Peptiden", Angew. Chem. 2006, 118, 4973-4976; Angew. Chem. Int. Ed. 2006, 45, 4855-4858.

91   U. Kazmaier, D. Stolz, "Regio- und stereoselektive Rhodium-katalysierte Allylische Alkylierungen chelatisierter Enolate", Angew. Chem. 2006, 118, 3143-3146; Angew. Chem. Int. Ed. 2006, 45, 3072-3075.

90   A. O. Wesquet, S. Dörrenbächer , U. Kazmaier, "Improved protocols for the molybdenum catalyzed hydrostannations of alkynes", Synlett 2006, 1105-1109.

89   U. Kazmaier, S. Lucas, M. Klein, "Syntheses and synthetic applications of stannylated allylic alcohols", J. Org. Chem. 2006, 71, 2429-2433.

88   U. Kazmaier, M. Bauer, "A new, modular approach towards 2-(1-hydroxyalkyl)­oxazolines, effective bidentate chiral ligands", J. Organomet. Chem. 2006, 691, 2155-2158.

87   S. Dörrenbächer, U. Kazmaier, S. Ruf, "A Straightforward Approach towards Piperidines via Stille Coupling and subsequent 1,4-Addition of Amines", Synlett 2006, 547-550.

86   S. Lucas, U. Kazmaier, "Allenyl ketones as versatile Michael acceptors for the addition of chelated enolates", Synlett 2006, 255-258.