Publikationen von Herbert Waldmann

Muller, G.; Lang, A.; Seithel, D.; Waldmann, H.: An enzyme-initiated hydroxylation-oxidation carbo Diels-Alder domino reaction. CHEMISTRY-A EUROPEAN JOURNAL 4 (12), S. 2513 - 2522 (1998)

Hinterding, K.; Knebel, A.; Herrlich, P.; Waldmann, H.: Synthesis and biological evaluation of aeroplysinin analogues: A new class of receptor tyrosine kinase inhibitors. BIOORGANIC & MEDICINAL CHEMISTRY 6 (8), S. 1153 - 1162 (1998)

Schene, H.; Waldmann, H.: Activation of glycosyl phosphites under neutral conditions in solutions of metal perchlorates in organic solvents. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (6), S. 1227 - 1230 (1998)

Schmittberger, T.; Waldmann, H.: Organic synthesis and biological signal transduction. SYNLETT (6), S. 574 - + (1998)

Schmid, U.; Waldmann, H.: Synthesis of fucosyl saccharides under neutral conditions in solutions of lithium perchlorate in dichloromethane. CHEMISTRY-A EUROPEAN JOURNAL 4 (3), S. 494 - 501 (1998)

Pathak, T.; Waldmann, H.: Enzymes and protecting group chemistry. CURRENT OPINION IN CHEMICAL BIOLOGY 2 (1), S. 112 - 120 (1998)

Brohm, D.; Waldmann, H.: Stereoselective synthesis of the core structure of the protein phosphatase inhibitor dysidiolide. TETRAHEDRON LETTERS 39 (23), S. 3995 - 3998 (1998)

Hinterding, K.; Alonso-Diaz, D.; Waldmann, H.: Organic synthesis and biological signal transduction. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 37 (6), S. 688 - 749 (1998)

Hinterding, K.; Hagenbuch, P.; Retey, J.; Waldmann, H.: Synthesis and in vitro evaluation of the Ras farnesyltransferase inhibitor pepticinnamin E. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 37 (9), S. 1236 - 1239 (1998)

Jungmann, V.; Waldmann, H.: An enzymatic protecting group strategy for the synthesis of nucleopeptides. TETRAHEDRON LETTERS 39 (10), S. 1139 - 1142 (1998)

Kirschbaum, S.; Waldmann, H.: Three-step access to the tricyclic benzo[a]quinolizine ring system. JOURNAL OF ORGANIC CHEMISTRY 63 (15), S. 4936 - 4946 (1998)

Nagele, E.; Schelhaas, M.; Kuder, N.; Waldmann, H.: Chemoenzymatic synthesis of N-Ras lipopeptides. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY 120 (28), S. 6889 - 6902 (1998)

Sauerbrei, B.; Jungmann, V.; Waldmann, H.: An enzyme-labile linker group for organic syntheses on solid supports. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 37 (8), S. 1143 - 1146 (1998)

Schene, H.; Waldmann, H.: Synthesis of 2-deoxy and 2,6-dideoxy glycosides under neutral conditions in LiClO4/Et2O mixtures. CHEMICAL COMMUNICATIONS (24), S. 2759 - 2760 (1998)

Schlede, U.; Nazare, M.; Waldmann, H.: Efficient enantioselective synthesis of a beta-hydroxyepoxide building block for the construction of macrocyclic natural products. TETRAHEDRON LETTERS 39 (10), S. 1143 - 1144 (1998)

Schmittberger, T.; Cotte, A.; Waldmann, H.: Synthesis of characteristic lipopeptides of lipid modified proteins employing the allyl ester as protecting group. CHEMICAL COMMUNICATIONS (8), S. 937 - 938 (1998)

Kappes, T.; Waldmann, H.: The tetrabenzylglucosyloxycarbonyl(BGloc)-group-A carbohydrate-derived enzyme-labile urethane protecting group. CARBOHYDRATE RESEARCH 305 (3-4), S. 341 - 349 (1997)

Schmid, U.; Waldmann, H.: O-glycoside synthesis with glycosyl iodides under neutral conditions in 1 M LiClO4 in CH2Cl2. LIEBIGS ANNALEN-RECUEIL (12), S. 2573 - 2577 (1997)

Schroeder, H.; Leventis, R.; Rex, S.; Schelhaas, M.; Nagele, E.; Waldmann, H.; Silvius, J.: The C-terminal sequence of mature N-ras is palmitoylated specifically at the plasma membrane in mammalian fibroblasts. MOLECULAR BIOLOGY OF THE CELL 8, S. 495 - 495 (1997)

Sebastian, D.; Heuser, A.; Schulze, S.; Waldmann, H.: Selective enzymatic removal of protecting groups from phosphopeptides: Chemoenzymatic synthesis of a characteristic phosphopeptide fragment of the Raf-1 kinase. Synthesis 1997 (9), S. 1098 - 1108 (1997)