Christian Noe, Dr. techn. - Publications

Affiliations: 
Institute of Pharmaceutical Chemistry Vienna University, Austria 

71 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Mehraban K, Gmeiner G, Urban E, Gärtner P, Eppacher S, Noe CR. Chiral resolution of alcohols by extractive separation of acetals Monatshefte FüR Chemie - Chemical Monthly. DOI: 10.1007/S00706-013-1139-8  0.555
2008 Berndt U, Stanetty C, Wanek T, Kuntner C, Stanek J, Berger M, Bauer M, Henriksen G, Wester HJ, Kvaternik H, Angelberger P, Noe C. Synthesis of a [18F]fluorobenzothiazole as potential amyloid imaging agent Journal of Labelled Compounds and Radiopharmaceuticals. 51: 137-145. DOI: 10.1002/Jlcr.1476  0.32
2004 Costantino G, Marinozzi M, Camaioni E, Natalini B, Sarichelou I, Micheli F, Cavanni P, Faedo S, Noe C, Moroni F, Pellicciari R. Stereoselective synthesis and preliminary evaluation of (+)- and (-)-3-methyl-5-carboxy-thien-2-yl-glycine (3-MATIDA): identification of (+)-3-MATIDA as a novel mGluR1 competitive antagonist. Farmaco (Societã  Chimica Italiana : 1989). 59: 93-9. PMID 14871500 DOI: 10.1016/J.Farmac.2003.11.008  0.305
2002 BINDER D, HABISON G, NOE C. (N-1)-t-Butoxycarbonyl-geschützte 2-Thienylhydrazine; II. Synthese der bisher nicht zugänglichen 2-Thienylpyrazolone Synthesis. 1978: 60-62. DOI: 10.1055/S-1978-25386  0.434
1999 Knollmüller M, Ferencic M, Gärtner P, Girreser U, Klinge M, Gaischin L, Mereiter K, Noe CR. 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.  0.731
1998 Knollmüller M, Gaischin L, Ferencic M, Noe-Letschnig M, Girreser U, Gärtner P, Mereiter K, Noe CR. Addition von enantiomerenreinen Aminen an aktivierte Olefine, 1. Mitt. Über die Addition an ω;-Nitrostyrol Monatshefte FüR Chemie / Chemical Monthly. 129: 1025-1033. DOI: 10.1007/Pl00010113  0.549
1998 Knollmüller M, Gaischin L, Ferencic M, Noe-Letschnig M, Girreser U, Gärtner P, Mereiter K, Noe CR. 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.  0.742
1998 Knollmüller M, Ferencic M, Gärtner P, Mereiter K, Noe CR. New camphor derived chiral ligands for asymmetric synthesis Tetrahedron Asymmetry. 9: 4009-4020.  0.732
1998 Knollmüller M, Gärtner P, Ferencic M, Noe CR, Mereiter K. An improved method for the endo-fusion of five-membered ring lactones to the bornane ring system European Journal of Organic Chemistry. 2507-2511.  0.71
1996 Noe CR, Knollmüller M, Gärtner P. 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.  0.705
1996 Noe CR, Knollmüller M, Völlenkle H, Noe-Letschnig M, Weigand A, Mühl J. Synthesis of α-alkylated 4-hydroxyprolines Pharmazie. 51: 800-804.  0.62
1996 Noe CR, Knollmüller M, Schödl C, Berger ML. 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.  0.583
1996 Noe CR, Knollmüller M, Gärtner P, Mereiter K, Steinbauer G. Chiral lactols, XIV: Stereoselective fusion of five-membered ring lactols to the bornane ring system Liebigs Annales. 1015-1021.  0.723
1996 Noe CR, Knollmüller M, Ziebarth-Schroth I, Letschnig M. Stereoelectronic effects and chiral recognition, II: Kinetic and thermodynamic control in the formation of chiral thioacetals and chiral thioethers Liebigs Annales. 1009-1013.  0.602
1995 Noe CR, Knollmüller M, Gärtner P, Fleischhacker W, Katikarides E. 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. DOI: 10.1007/Bf00813211  0.707
1995 Noe CR, Knollmüller M, Gärtner P, Fleischhacker W, Katikarides E. Aminoalcohols III: Preparation of enantiomerically pure pharmacologically active N-substituted β-aminoalcohols | Aminoalkohole, 3. Mitt. Ein Verfahren zur Herstellung von enantiomerenreinen pharmakologisch aktiven N-substituierten β-Aminoalkoholen Monatshefte FüR Chemie Chemical Monthly. 126: 557-564. DOI: 10.1007/Bf00807429  0.716
1995 Noe CR, Knollmüller M, Gärtner P, Katikarides E, Gaischin L, Völlenkle H. Chiral lactols, XIII. On the determination of the absolute configuration of aromatic cyanohydrins and structurally related compounds Liebigs Annalen. 1995: 1353-1360. DOI: 10.1002/jlac.1995199507180  0.642
1991 Wagner E, Oberhauser B, Holzner A, Brunar H, Issakides G, Schaffner G, Cotten M, Knollmüller M, Noe CR. A simple procedure for the preparation of protected 2'-O-methyl or 2'-O-ethyl ribonucleoside-3'-O-phosphoramidites. Nucleic Acids Research. 19: 5965-71. PMID 1945882 DOI: 10.1093/nar/19.21.5965  0.611
1991 Noe CR, Knollmüller M, Dungler K, Miculka C, Gärtner P. A method for the synthesis of enantiomerically pure alkanols by reductive desulfurization of thiophene-alcohols | Ein Verfahren zur Synthese enantiomerenreiner Alkanole durch reduktive Entschwefelung von Thiophenalkoholen Monatshefte FüR Chemie Chemical Monthly. 122: 705-718. DOI: 10.1007/Bf00811470  0.745
1991 Noe CR, Knollmüller M, Steinbauer G, Wagner E, Kürner H, Ettmayer P, Völlenkle H. Pheromones, III: A simple method to direct the reduction of α-alkoxy-carbonyl compounds | Pheromone, 3.Mitt.: Eine einfache Methode zur Steuerung der Reduktion von α-Alkoxy-carbonylverbindungen Monatshefte FüR Chemie Chemical Monthly. 122: 299-317. DOI: 10.1007/BF00810831  0.614
1991 Noe CR, Knollmüller M, Göstl G, Gärtner P. Amino-Alcohols, I: A method for the synthesis of enantiomerically pure 1,2-aminoalcohols with erythro-configuration | Aminoalkohole, 1. Mitt.: Ein Verfahren zur Synthese enantiomerenreiner 1,2-Aminoalkohole mit erythro-Konfiguration Monatshefte FüR Chemie Chemical Monthly. 122: 283-290. DOI: 10.1007/BF00810829  0.726
1991 Noe CR, Knollmüller M, Dungler K, Gärtner P. A method for the synthesis of ketones and spiroketals via desulfurization of thienylethers | Pheromone, 2. Mitt. Ein Verfahren zur Herstellung von Ketonen und Spiroketalen durch Entschwefelung von Thienylethern Monatshefte FüR Chemie Chemical Monthly. 122: 185-194. DOI: 10.1007/BF00809364  0.737
1990 Binder D, Noe CR, Holzer W. Thiophene as a structural element of physiologically active compounds, XVII: A thiophene analogue of propafenon | THIOPHEN ALS STRUKTURELEMENT PHYSIOLOGISCH AKTIVER SUBSTANZEN, 18. MITT.(1)): EIN THIOPHENANALOGON DES PROPAFENONS Archiv Der Pharmazie. 323: 919-921. PMID 2080899 DOI: 10.1002/ardp.19903231108  0.528
1988 Binder D, Noe CR, Baumann K, Holzer W. Thiophene as a structural element in physiologically active substances. 17. Thienoisoxazoles through nucleophile substitution | Thiophen als Strukturelement physiologisch aktiver Substanzen, 17. Mitt. Thienoisoxazole durch nukleophile Substitution Archiv Der Pharmazie. 321: 391-395. PMID 3219055 DOI: 10.1002/Ardp.19883210704  0.53
1988 BINDER D, NOE CR, HOLZER W, BAUMANN K. ChemInform Abstract: Thiophene as a Structural Element of Physiologically Active Compounds. Part 16. Thienoisoxazoles by Substitution at the Oxime Nitrogen. Cheminform. 19. DOI: 10.1002/chin.198806150  0.553
1988 Noe CR, Knollmüller M, Ettmayer P. Paraformaldehyde as Possible Chirality Amplifier Angewandte Chemie International Edition in English. 27: 1379-1381. DOI: 10.1002/anie.198813791  0.6
1987 Binder D, Noe CR, Holzer W, Baumann K. Thiophene as a structural element of physiologically active compounds. 16. Thienoisoxazoles by substitution at the oxime nitrogen | Thiophen als Strukturelement physiologisch aktiver Substanzen, 16. Mitt. Thienoisoxazole durch Substitution am Oximstickstoff Archiv Der Pharmazie. 320: 837-843. PMID 3675172 DOI: 10.1002/Ardp.19873200911  0.556
1987 Binder D, Hromatka O, Geissler F, Schmied K, Noe CR, Burri K, Pfister R, Strub K, Zeller P. Analogues and derivatives of tenoxicam. 1. Synthesis and antiinflammatory activity of analogues with different residues on the ring nitrogen and the amide nitrogen. Journal of Medicinal Chemistry. 30: 678-82. PMID 3494124 DOI: 10.1021/Jm00387A017  0.691
1986 Noe CR, Knollmüller M, Wagner E. A simple method for the synthesis of fused thiophenes | Ein einfaches Verfahren zur Herstellung anellierter Thiophene Monatshefte FüR Chemie Chemical Monthly. 117: 621-629. DOI: 10.1007/BF00817900  0.632
1986 Knollmüller M, Noe CR, Oberhauser B. The acetal group, I. Acetals of halomethyl-arylcarbinols | Die Acetalgruppe, 1. Mitt. Acetale von Halogenmethyl-arylcarbinolen Monatshefte FüR Chemie Chemical Monthly. 117: 407-419. DOI: 10.1007/BF00816535  0.571
1985 Binder D, Noe CR, Leitner A. Thiophene as a structural element of physiologically active compounds, XIV. The synthesis of 5-[5-methyl-3-thienyl)oxy]-2(1H)-pyrimidinon | THIOPHEN ALS STRUKTURELEMENT PHYSIOLOGISCHE AKTIVER SUBSTANZEN, 14. Mitt. DIE SYNTHESE VON 5-[(5-methyl-3-thienyl)oxy]-2(1H)-pyrimidinon Archiv Der Pharmazie. 318: 210-213. PMID 4015338 DOI: 10.1002/Ardp.19853180305  0.575
1985 Binder D, Noe CN, Holzer W, Rosenwirth B. Thiophene as a structural element of physiologically active compounds. XIII: Thiophene analogues of antiviral flavanes | THIOPHEN ALS STRUKTURELEMENT PHYSIOLOGISCH AKTIVER SUBSTANZEN. 13. MITT. THIOPHENANALOGA ANTIVIRALER FLAVANE Archiv Der Pharmazie. 318: 70-78. PMID 2985025 DOI: 10.1002/Ardp.19853180113  0.532
1985 Binder D, Noe CR, Kollmann H, Rosenwirth B. Thiophene as a structural element of physiologically active compounds. XI: Substituted thieno[2,3-d]imidazoles as potentially antiviral compounds | SUBSTITUIERTE THIENO[2,3-d]IMIDAZOLE ALS POTENTIELL ANTIVIRALE WIRKSTOFFE Archiv Der Pharmazie. 318: 40-48. PMID 2985023 DOI: 10.1002/ardp.19853180110  0.516
1985 Binder D, Noe CR, Baumann K, Wildburger JMF. Thiopene as a structural element of physiologically active compounds, XV: The thiophene analogue of an anxiolytically active 1,2,4-triazolo[4,3,-b]pyridazine | THIOPHEN ALS STRUKTURELEMENT PHYSIOLOGISCHE AKTIVER SUBSTANZEN, 15. MITT. DAS THIOPHENANALOGON EINES ANXIOLYTISCH WIRKSAMEN 1,2,4-TRIAZOLO[4,3-b]PYRIDAZINS Archiv Der Pharmazie. 318: 243-249. PMID 2861800 DOI: 10.1002/Ardp.19853180312  0.541
1985 BINDER D, NOE CR, LEITNER A. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE COMPOUNDS, XIV. SYNTHESIS OF 5-((5-METHYL-3-THIENYL)OXY)-2(1H)-PYRIMIDINONE Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198526247  0.568
1985 BINDER D, NOE CR, BAUMANN K, WILDBURGER JMF. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE COMPOUNDS, XV. THIOPHENE ANALOG OF AN ANXIOLYTICALLY ACTIVE 1,2,4-TRIAZOLO(4,3-B)PYRIDAZINE Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198526244  0.53
1985 BINDER D, NOE CR, HOLZER W, ROSENWIRTH B. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE SUBSTANCES, XIII. THIOPHENE ANALOGS OF ANTIVIRAL FLAVANS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198519213  0.498
1985 BINDER D, NOE CR, KOLLMANN H, ROSENWIRTH B. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE SUBSTANCES, XI. SUBSTITUTED THIENO(2,3-D)IMIDAZOLES AS POTENTIALLY ANTIVIRAL AGENTS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198519205  0.5
1985 BINDER D, NOE CR, HOLZER W, ROSENWIRTH B. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE SUBSTANCES, XII. THIOPHENE ANALOGS OF ANTIVIRAL CHALCONES Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198519194  0.499
1985 Noe CR, Knollmüller M, Wagner E, Völlenkle H. Kohlenhydrat-Modelle, I. Kinetische und thermodynamische Effekte bei Acetalisierungsreaktionen enantiomerenreiner Thiolactole Chemische Berichte. 118: 3299-3310. DOI: 10.1002/cber.19851180829  0.537
1985 Noe CR, Knollmüller M, Wagner E, Völlenkle H. Chirale Lactole, IV. Selektivitäten bei Acetalisierungsreaktionen enantiomerenreiner Lactole am Beispiel von Octahydro-8,9,9-trimethyl-5,8-methano-2H-1-benzopyran-2-ol Chemische Berichte. 118: 1733-1745. DOI: 10.1002/cber.19851180502  0.613
1985 Binder D, Noe CR, Holzer W, Rosenwirth B. Thiophen als Strukturelement physiologisch aktiver Substanzen, 12. Mitt. Thiophenanaloga antiviraler Chalkone Archiv Der Pharmazie. 318: 48-59. DOI: 10.1002/Ardp.19853180111  0.549
1983 BINDER D, NOE CR, PRAGER BC, TURNOWSKY F. ChemInform Abstract: PYRAZINE-1,4-DIOXIDES FUSED TO HETEROCYCLES. 3. SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF SUBSTITUTED PTERIDINE-5,8-DIOXIDES Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198341247  0.561
1982 BINDER D, GEORGOPOULOS A, NOE CR, NUSSBAUMER J, PRAGER BC, TURNOWSKY F. ChemInform Abstract: PYRAZINE-1,4-DIOXIDES FUSED TO HETEROCYCLES. 2. SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF SUBSTITUTED PYRIDO(2,3-B)PYRAZINE-1,4-DIOXIDES Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198221226  0.543
1982 BINDER D, NOE CR, PRAGER BC. ChemInform Abstract: THIOPHENE AS STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE COMPOUNDS, X: SUBSTITUTED 3-ALKOXY-4,5,6,7-TETRAHYDRO-8H-THIENO(2,3-B)INDOLES Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198212236  0.542
1981 BINDER D, NOE CR, GEISSLER F, HILLEBRAND F. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE SUBSTANCES. PART 9. THIENOPYRAZINE 1,4-DIOXIDES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198141218  0.488
1981 BINDER D, NOE CR, ZAHORA M. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE SUBSTANCES. PART 8. 1H,5H-IMIDAZO(1,2-A)THIENO(3,4-D)PYRIMIDIN-2(3H)-ONES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198139240  0.481
1981 BINDER D, PRAGER BC, NOE CR. ChemInform Abstract: N1-TERT-BUTOXYCARBONYL-2-THIENYLHYDRAZINES. PART 3. INFLUENCE OF A METHOXY GROUP IN THE FISCHER REACTION Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198135236  0.446
1981 BINDER D, HROMATKA O, NOE CR, HILLEBRAND F, VEIT W. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE SUBSTANCES. IV: O-SUBSTITUTED 5-PHENYLTHIENO(2,3-E)(1,4)DIAZEPINES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198102280  0.666
1981 BINDER D, HROMATKA O, NOE CR, BARA YA, FEIFEL M, HABISON G, LEIERER F, BLUM JE. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE SUBSTANCES. V: 5-(O-NITROPHENYL)THIENO(2,3-E)(1,4)DIAZEPINES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198102279  0.648
1981 Binder D, Noe CR, Prager BC. Thiophen als Strukturelement physiologisch aktiver Substanzen, 10. Mitt. Substituierte 3-Alkoxy-4,5,6,7-tetrahydro-8H-thieno[2,3-b]indole Archiv Der Pharmazie. 314: 751-757. DOI: 10.1002/Ardp.19813140905  0.568
1981 Binder D, Noe CR, Geißler F, Hillebrand F. Thiophen als Strukturelement physiologisch aktiver Substanzen, 9. Mitt. Thienopyrazin-1,4-dioxide Archiv Der Pharmazie. 314: 564-567. DOI: 10.1002/Ardp.19813140614  0.565
1981 Binder D, Noe CR, Zahora M. Thiophen als Strukturelement physiologisch aktiver Substanzen, 8. Mitt. 1H,5H-Imidazo[1,2-a]thieno[3,4-d]pyrimidin-2(3H)-one Archiv Der Pharmazie. 314: 557-564. DOI: 10.1002/Ardp.19813140613  0.521
1980 Binder D, Hromatka O, Noe CR, Hillebrand F, Veit W, Blum JE. [Thiophene as a structural element of physiologically active compounds, IV: o-Substituted 5-phenylthieno(2,3-e)(1,4)diazepines (author's transl)]. Archiv Der Pharmazie. 313: 587-602. PMID 7406668 DOI: 10.1002/Ardp.19803130704  0.698
1980 Binder D, Hromatka O, Noe CR, Bara YA, Feifel M, Habison G, Leierer F, Blum JE. [Thiophene as a structural element of physiologically active compounds, V:5(o-Nitrophenyl)thieno(2,3-e][1,4]diazepines (author's transl)]. Archiv Der Pharmazie. 313: 636-44. PMID 7190816 DOI: 10.1002/Ardp.19803130708  0.689
1980 Binder D, Noe CR, Nußbaumer J, Prager BC. Pyrazine-1,4-dioxides fused to heterocycles; I.: The positionsselective synthesis of pyrido[2,3-d]pyrazine-1,4-dioxides | Heterocyclisch anellierte Pyrazin-1,4-dioxide; 1. Mitt.: Die positionsselektive Synthese von Pyrido[2,3-b]pyrazin-1,4-dioxiden Monatshefte FüR Chemie. 111: 407-411. DOI: 10.1007/Bf00903236  0.556
1980 BINDER D, NOE CR, NUSSBAUMER J, PRAGER BC. ChemInform Abstract: HETEROCYCLIC FUSED PYRAZINE-1,4-DIOXIDES. PART 1. POSITION-SELECTIVE SYNTHESIS OF PYRIDO(2,3-D)PYRAZINE-1,4-DIOXIDES Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198031232  0.487
1980 BINDER D, NOE CR, HABISON G. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE COMPOUNDS. PART 3. HIENYLPYRAZOLONES Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198005239  0.529
1980 BINDER D, NOE CR, HILLEBRAND F. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE COMPOUNDS. PART 2. HE SYNTHESIS OF BASE-SUBSTITUTED 3H-THIENO(2,3-D)IMIDAZOLES Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198005238  0.573
1979 BINDER D, HILLEBRAND F, NOE CR. ChemInform Abstract: SYNTHESIS OF SUBSTITUTED THIENO(2,3-D)IMIDAZOLES Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197929243  0.515
1979 BINDER D, NOE CR, HABISON G, CHOCHOLOUS J. ChemInform Abstract: THIOPHENE AS A STRUCTURAL ELEMENT OF PHYSIOLOGICALLY ACTIVE COMPOUNDS, I: SYNTHESIS OF DERIVATIVES OF 4-THIENO(2,3-B)PYRROLEACETIC ACID Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197925203  0.561
1978 BINDER D, HABISON G, NOE CR. ChemInform Abstract: (N-1)-TERT-BUTOXYCARBONYL PROTECTED 2-THIENYLHYDRAZINES, II. SYNTHESIS OF PREVIOUSLY INACCESSIBLE 2-THIENYLPYRAZOLONES Chemischer Informationsdienst. 9. DOI: 10.1002/Chin.197818180  0.493
1977 BINDER D, HABISON G, NOE CR. N 1-t-Butoxycarbonyl-geschützte 2-Thienylhydrazine; I. Herstellung von Thieno[2,3-b]pyrrolen mittels "Fischer"-Indolsynthese Synthesis. 1977: 487-489. DOI: 10.1055/S-1977-24456  0.412
1977 BINDER D, HABISON G, NOE CR. Eine einfache Herstellungsmethode für 2-Aminothiophene Synthesis. 1977: 255-256. DOI: 10.1055/S-1977-24341  0.433
1977 Binder D, Noe CR. Preparation of 4-oxofluorenes part 2. The synthesis of 8-methoxy-1,2,3,9-tetrahydro-4-fluorenone | Die Synthese von 8-Methoxy-1,2,3,9-tetrahydro-4-fluorenon - Zur Herstellung von 4-Fluorenonen, 2. Mitt Monatshefte FüR Chemie. 108: 839-851. DOI: 10.1007/Bf00898049  0.568
1977 BINDER D, HABISON G, NOE CR. ChemInform Abstract: N1-TERT-BUTOXYCARBONYL-PROTECTED 2-THIENYLHYDRAZINES, I. PREPARATION OF THIENO(2,3-B)PYRROLES USING FISHER INDOLE SYNTHESIS Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/Chin.197744226  0.516
1977 BINDER D, HABISON G, NOE CR. ChemInform Abstract: A SIMPLE METHOD FOR THE PREPARATION OF 2-AMINOTHIOPHENES Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/Chin.197731174  0.481
1976 Binder D, Noe CR. Preparation of 4-fluorenones-An intramolecular ring closure reaction of the indenyl anion | Zur Herstellung von 4-Fluorenonen-eine intramolekulare Ringschlußreaktion am Indenylanion Monatshefte FüR Chemie. 107: 1145-1151. DOI: 10.1007/Bf00903801  0.528
1973 Hromatka O, Binder D, Noe CR, Stanetty P, Veit W. Synthesis of substituted 5-phenyl-1H-thieno[2.3-e]1.4-diazepin-2(3H)-ones | Über die Synthese von substituierten 5-Phenyl-1 H-thieno[2,3-e]1,4-diazepin-2(3 H)-onen Monatshefte FüR Chemie. 104: 715-721. DOI: 10.1007/Bf00910583  0.644
1973 Binder D, Noe CR. Synthesis of in position 5 halogenated, in the aromatic nucleus substituted valerophenones | Über die synthese von in position 5 halogenierten, im aromatischen Kern substituierten Valerophenonen Monatshefte FüR Chemie. 104: 1097-1100. DOI: 10.1007/BF00903927  0.503
1973 HROMATKA O, BINDER D, NOE CR, STANETTY P, VEIT W. ChemInform Abstract: SYNTH. VON SUBSTITUIERTEN 5-PHENYL-1H-THIENO(2,3-E)1,4-DIAZEPIN-2(3H)-ONEN Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197334306  0.624
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