Publikationen von Herbert Waldmann

Lock, R.; Waldmann, H.: Enantioselective construction of highly functionalized indoloquinolizines - Congeners to polycyclic indole alkaloids. CHEMISTRY-A EUROPEAN JOURNAL 3 (1), S. 143 - 151 (1997)

Pohl, T.; Waldmann, H.: Chemoenzymatic synthesis of a characteristic phosphorylated and glycosylated peptide fragment of the large subunit of mammalian RNA polymerase II. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY 119 (29), S. 6702 - 6710 (1997)

Schroeder, H.; Leventis, R.; Rex, S.; Schelhaas, M.; Nagele, E.; Waldmann, H.; Silvius, J.: S-acylation and plasma membrane targeting of the farnesylated carboxyl-terminal peptide of N-ras in mammalian fibroblasts. BIOCHEMISTRY 36 (42), S. 13102 - 13109 (1997)

Sebastian, D.; Waldmann, H.: Chemoenzymatic synthesis of a characteristic phosphopeptide fragment of the Raf-1 kinase. TETRAHEDRON LETTERS 38 (17), S. 2927 - 2930 (1997)

Stober, P.; Schelhaas, M.; Nagele, E.; Hagenbuch, P.; Retey, J.; Waldmann, H.: Synthesis of characteristic lipopeptides of the human N-Ras protein and their evaluation as possible inhibitors of protein farnesyl transferase. BIOORGANIC & MEDICINAL CHEMISTRY 5 (1), S. 75 - 83 (1997)

Waldmann, H.: Bioorganic chemistry of signal transduction - Preface. BIOORGANIC & MEDICINAL CHEMISTRY 5 (1), S. R9 - R9 (1997)

Waldmann, H.; Gabold, S.: Chemoenzymatic synthesis of nucleopeptides. CHEMICAL COMMUNICATIONS 1997 (19), S. 1861 - 1862 (1997)

Waldmann, H.; Hinterding, K.; Herrlich, P.; Rahmsdorf, H.; Knebel, A.: Selective inhibition of receptor tyrosine kinases by synthetic analogues of aeroplysinin. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 36 (13-14), S. 1541 - 1542 (1997)

Waldmann, H.; Reidel, A.: The phenylacetyl group - The first amino protecting group that can be removed enzymatically from oligonucleotides in solution and on a solid support. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 36 (6), S. 647 - 649 (1997)

Waldmann, H.; Schelhaas, M.; Nagele, E.; Kuhlmann, J.; Wittinghofer, A.; Schroeder, H.; Silvius, J.: Chemoenzymatic synthesis of fluorescent N-ras lipopeptides and their use in membrane localization studies in vivo. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 36 (20), S. 2238 - 2241 (1997)

Schmidt, G.; Waldmann, H.; Henke, H.; Burkard, M.: Asymmetric control in the Pictet-Spengler reaction by means of N-protected amino acids as chiral auxiliary groups. CHEMISTRY-A EUROPEAN JOURNAL 2 (12), S. 1566 - 1571 (1996)

Bohm, G.; Waldmann, H.: O-glycoside synthesis under neutral conditions in concentrated solutions of LiClO4 in organic solvents employing benzyl-protected glycosyl donors. LIEBIGS ANNALEN (4), S. 613 - 619 (1996)

Bohm, G.; Waldmann, H.: O-glycoside synthesis under neutral conditions in concentrated solutions of LiClO4 in organic solvents employing O-acyl-protected glycosyl donors. LIEBIGS ANNALEN (4), S. 621 - 625 (1996)

Lock, R.; Waldmann, H.: Asymmetric synthesis of highly functionalized tetracyclic indole bases embodying the basic skeleton of yohimbine- and reserpine type alkaloids. TETRAHEDRON LETTERS 37 (16), S. 2753 - 2756 (1996)

Muller, G.; Waldmann, H.: An enzyme-initiated domino hydroxylation-oxidation carbo Diels-Alder reaction cascade. TETRAHEDRON LETTERS 37 (22), S. 3833 - 3836 (1996)

Pohl, T.; Waldmann, H.: Enzymatic synthesis of a characteristic phosphorylated and glycosylated peptide fragment of the large subunit of mammalian RNA polymerase II. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 35 (15), S. 1720 - 1723 (1996)

Schelhaas, M.; Glomsda, S.; Hansler, M.; Jakubke, H.; Waldmann, H.: Enzymatic synthesis of peptides and Ras lipopeptides employing choline ester as a solubilizing, protecting, and activating group. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 35 (1), S. 106 - 109 (1996)

Schelhaas, M.; Waldmann, H.: Protecting group strategies in organic synthesis. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 35 (18), S. 2056 - 2083 (1996)

Schmid, U.; Waldmann, H.: Activation of glycosyl phosphates by in situ conversion to glycosyl iodides under neutral conditions in concentrated solutions of lithium perchlorate in organic solvents. TETRAHEDRON LETTERS 37 (22), S. 3837 - 3840 (1996)

Waldmann, H.; Heuser, A.; Schulze, S.: Selective enzymatic removal of protecting groups: The phenylacetamide as amino protecting group in phosphopeptide synthesis. TETRAHEDRON LETTERS 37 (48), S. 8725 - 8728 (1996)