Max Knollmüller, Dr. techn.
Affiliations: | Organic Chemistry | TU Vienna |
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| Knollmüller M, Ferencic M, Gärtner P, et al. (1999) Addition of enantiomerically pure amines to activated olefines II. On the addition to ethyl (E)-4-oxo-4-phenyl-2-butenoate | Addition von enantiomerenreinen aminen an aktivierte olefine, 2. mitt. über die addition an (E)-4-oxo-4-phenyl-2-butensäure-ethylester Monatshefte Fur Chemie. 130: 769-782 |
| Knollmüller M, Gaischin L, Ferencic M, et al. (1998) Addition of enantiomerically pure amines to activated olefins I. On the addition to ω-nitrostyrene | Addition von enantiomerenreinen aminen an aktivierte olefine, 1. Mitt. Über die addition an ω-nitrostyrol Monatshefte Fur Chemie. 129: 1025-1033 |
| Knollmüller M, Ferencic M, Gärtner P, et al. (1998) New camphor derived chiral ligands for asymmetric synthesis Tetrahedron Asymmetry. 9: 4009-4020 |
| Knollmüller M, Gärtner P, Ferencic M, et al. (1998) An improved method for the endo-fusion of five-membered ring lactones to the bornane ring system European Journal of Organic Chemistry. 2507-2511 |
| Noe CR, Knollmüller M, Ziebarth-Schroth I, et al. (1996) Stereoelectronic effects and chiral recognition, II: Kinetic and thermodynamic control in the formation of chiral thioacetals and chiral thioethers Liebigs Annales. 1009-1013 |
| Noe CR, Knollmüller M, Gärtner P, et al. (1996) Chiral lactols, XIV: Stereoselective fusion of five-membered ring lactols to the bornane ring system Liebigs Annales. 1015-1021 |
| Noe CR, Knollmüller M, Schödl C, et al. (1996) 2,3-Dihydro-2-carboxy-1H-indole-3-acetic acids as tools for the study of excitatory amino acid receptors | 2,3-Dihydro-2-carboxy-1H-indol-3-essigsauren als Sonden zur Untersuchung exzitatorischer Aminosaurerezeptoren Scientia Pharmaceutica. 64: 577-590 |
| Noe CR, Knollmüller M, Völlenkle H, et al. (1996) Synthesis of α-alkylated 4-hydroxyprolines Pharmazie. 51: 800-804 |
| Noe CR, Knollmüller M, Gärtner P. (1996) A Separation Procedure for the Preparation of Enantiomerically Pure Midodrine | Aminoalkohole, 4. Mitt. [1]: Ein Trennverfahren zur Herstellung von enantiomerenreinem Midodrin Monatshefte Fur Chemie. 127: 159-165 |
| Noe CR, Knollmüller M, Gärtner P, et al. (1995) Aminoalcohols II: Preparation of enantiomerically pure pharmacologically active β-aminoalcohols | Aminoalkohole, 2. Mitt.: Ein Verfahren zur Herstellung enantiomerenreiner pharmakologisch aktiver β-Aminoalkohole Monatshefte FüR Chemie Chemical Monthly. 126: 481-494 |