| Year |
Citation |
Score |
| 2012 |
Schareina T, Wu XF, Zapf A, Cotté A, Gotta M, Beller M. Towards a practical and efficient copper-catalyzed trifluoromethylation of aryl halides Topics in Catalysis. 55: 426-431. DOI: 10.1007/S11244-012-9824-0 |
0.623 |
|
| 2011 |
Schareina T, Zapf A, Cotte A, Gotta M, Beller M. ChemInform Abstract: A Versatile Protocol for Copper-Catalyzed Cyanation of Aryl and Heteroaryl Bromides with Acetone Cyanohydrin. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201128066 |
0.505 |
|
| 2011 |
Schareina T, Zapf A, Cotté A, Gotta M, Beller M. A versatile protocol for copper-catalyzed cyanation of aryl and heteroaryl bromides with acetone cyanohydrin Advanced Synthesis and Catalysis. 353: 777-780. DOI: 10.1002/Adsc.201000200 |
0.583 |
|
| 2010 |
Zapf A, Beller M. ChemInform Abstract: Fine Chemical Synthesis with Homogeneous Palladium Catalysts: Examples, Status and Trends Cheminform. 33: no-no. DOI: 10.1002/CHIN.200251275 |
0.4 |
|
| 2010 |
Andreu MG, Zapf A, Beller M. ChemInform Abstract: Synthesis and Catalytic Application of 1,6-Diene-palladium(0) Monophosphine Complexes Cheminform. 33: no-no. DOI: 10.1002/CHIN.200249211 |
0.364 |
|
| 2010 |
Sundermeier M, Zapf A, Beller M, Sans J. ChemInform Abstract: Palladium-Catalyzed Reactions for Fine Chemical Synthesis. Part 21. A New Palladium Catalyst System for the Cyanation of Aryl Chlorides. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200150086 |
0.625 |
|
| 2010 |
BELLER M, ZAPF A. ChemInform Abstract: Palladium-Catalyzed Reactions for Fine Chemical Synthesis. Part 5. Phosphites as Ligands for Efficient Catalysis of Heck Reactions. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199843069 |
0.458 |
|
| 2010 |
RIERMEIER TH, ZAPF A, BELLER M. ChemInform Abstract: Palladium-Catalyzed Reactions for Fine Chemical Synthesis.Part 3. Palladium-Catalyzed C-C- and C-N Coupling Reactions of Aryl Chlorides Cheminform. 29: no-no. DOI: 10.1002/CHIN.199828332 |
0.394 |
|
| 2010 |
Schareina T, Zapf A, Cotté A, Gotta M, Beller M. An improved protocol for palladium-catalyzed alkoxycarbonylations of aryl chlorides with alkyl formates Advanced Synthesis and Catalysis. 352: 1205-1209. DOI: 10.1002/Adsc.201000047 |
0.622 |
|
| 2009 |
Torborg C, Huang J, Schulz T, Schäffner B, Zapf A, Spannenberg A, Börner A, Beller M. Improved palladium-catalyzed Sonogashira coupling reactions of aryl chlorides. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 1329-36. PMID 19123225 DOI: 10.1002/Chem.200802444 |
0.622 |
|
| 2009 |
Schulz T, Torborg C, Schäffner B, Huang J, Zapf A, Kadyrov R, Börner A, Beller M. Practical imidazole-based phosphine ligands for selective palladium-catalyzed hydroxylation of aryl halides Angewandte Chemie - International Edition. 48: 918-921. PMID 19105168 DOI: 10.1002/Anie.200804898 |
0.571 |
|
| 2009 |
Torborg C, Huang J, Schulz T, Schäffner B, Zapf A, Spannenberg A, Borner A, Beller M. Improved palladium-catalyzed sonogashira coupling reactions of aryl chlorides Chemistry - a European Journal. 15: 1329-1336. DOI: 10.1002/chem.200802444 |
0.569 |
|
| 2009 |
Schareina T, Jackstell R, Schulz T, Zapf A, Cotté A, Gotta M, Beller M. Increasing the scope of palladium-catalyzed cyanations of aryl chlorides Advanced Synthesis and Catalysis. 351: 643-648. DOI: 10.1002/Adsc.200800733 |
0.54 |
|
| 2008 |
Torborg C, Zapf A, Beller M. Palladium catalysts for highly selective Sonogashira reactions of aryl and heteroaryl bromides. Chemsuschem. 1: 91-6. PMID 18605670 DOI: 10.1002/Cssc.200700004 |
0.655 |
|
| 2008 |
Schareina T, Zapf A, Cotté A, Müller N, Beller M. A bio-inspired copper catalyst system for practical catalytic cyanation of aryl bromides Synthesis. 3351-3355. DOI: 10.1055/S-0028-1083161 |
0.589 |
|
| 2008 |
Schareina T, Zapf A, Cotté A, Müller N, Beller M. A practical and improved copper-catalyzed synthesis of the central intermediate of diafenthiuron and related products Organic Process Research and Development. 12: 537-539. DOI: 10.1021/Op700287S |
0.607 |
|
| 2008 |
Sergeev AG, Zapf A, Spannenberg A, Beller M. Synthesis and crystal structure of palladium(0) and arylpalladium (II) bromide complexes of CataCXium A Organometallics. 27: 297-300. DOI: 10.1021/Om700889B |
0.487 |
|
| 2008 |
Schareina T, Zapf A, Cotté A, Müller N, Beller M. Bio-inspired copper catalysts for the formation of diaryl ethers Tetrahedron Letters. 49: 1851-1855. DOI: 10.1016/J.Tetlet.2008.01.036 |
0.628 |
|
| 2008 |
Schareina T, Zapf A, Cotte A, Mueller N, Beller M. ChemInform Abstract: A Practical and Improved Copper-Catalyzed Synthesis of the Central Intermediate (IIIa) of Diafenthiuron (IV) and Related Products. Cheminform. 39. DOI: 10.1002/CHIN.200839069 |
0.437 |
|
| 2008 |
Schareina T, Zapf A, Cotte A, Mueller N, Beller M. ChemInform Abstract: Bio-Inspired Copper Catalysts for the Formation of Diaryl Ethers. Cheminform. 39. DOI: 10.1002/CHIN.200826076 |
0.5 |
|
| 2008 |
Kischel J, Mertins K, Jovel I, Zapf A, Beller M. Iron-Catalyzed Aromatic Substitutions Iron Catalysis in Organic Chemistry: Reactions and Applications. 177-196. DOI: 10.1002/9783527623273.ch6 |
0.369 |
|
| 2007 |
Kischel J, Michalik D, Zapf A, Beller M. FeCl3-catalyzed addition of 1,3-dicarbonyl compounds to aromatic olefins. Chemistry, An Asian Journal. 2: 909-14. PMID 17568471 DOI: 10.1002/Asia.200700055 |
0.611 |
|
| 2007 |
Schareina T, Zapf A, Mägerlein W, Müller N, Beller M. A state-of-the-art cyanation of aryl bromides: a novel and versatile copper catalyst system inspired by Nature. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 6249-54. PMID 17480048 DOI: 10.1002/Chem.200700079 |
0.581 |
|
| 2007 |
Beller M, Schareina T, Zapf A, Mägerlein W, Müller N. Pd-Catalyzed Cyanation of Aryl Chlorides with K4[Fe(CN)6] Synfacts. 2007: 0416-0416. DOI: 10.1055/S-2007-968328 |
0.355 |
|
| 2007 |
Schareina T, Zapf A, Mägerlein W, Müller N, Beller M. Copper-catalyzed cyanation of heteroaryl bromides: A novel and versatile catalyst system inspired by nature Synlett. 555-558. DOI: 10.1055/s-2007-967979 |
0.543 |
|
| 2007 |
Schareina T, Zapf A, Maegerlein W, Mueller N, Beller M. Copper-Catalyzed Cyanation of Heteroaryl Bromides: A Novel and Versatile Catalyst System Inspired by Nature. Cheminform. 38. DOI: 10.1055/S-2007-967979 |
0.594 |
|
| 2007 |
Schareina T, Zapf A, Mägerlein W, Müller N, Beller M. A new palladium catalyst system for the cyanation of aryl chlorides with K4[Fe(CN)6] Tetrahedron Letters. 48: 1087-1090. DOI: 10.1016/j.tetlet.2006.12.087 |
0.454 |
|
| 2007 |
Schareina T, Zapf A, Maegerlein W, Mueller N, Beller M. A New Palladium Catalyst System for the Cyanation of Aryl Chlorides with K4[Fe(CN)6]. Cheminform. 38. DOI: 10.1016/J.Tetlet.2006.12.087 |
0.652 |
|
| 2007 |
Kischel J, Mertins K, Michalik D, Zapf A, Beller M. A General and Efficient Iron-Catalyzed Benzylation of 1,3-Dicarbonyl Compounds. Cheminform. 38. DOI: 10.1002/CHIN.200733044 |
0.363 |
|
| 2007 |
Kischel J, Mertins K, Michalik D, Zapf A, Beller M. A general and efficient iron-catalyzed benzylation of 1,3-dicarbonyl compounds Advanced Synthesis and Catalysis. 349: 865-870. DOI: 10.1002/Adsc.200600497 |
0.546 |
|
| 2006 |
Kischel J, Jovel I, Mertins K, Zapf A, Beller M. A convenient FeCl3-catalyzed hydroarylation of styrenes. Organic Letters. 8: 19-22. PMID 16381557 DOI: 10.1021/ol0523143 |
0.517 |
|
| 2006 |
Klaus S, Neumann H, Zapf A, Strübing D, Hübner S, Almena J, Riermeier T, Groß P, Sarich M, Krahnert W, Rossen K, Beller M. Eine allgemeine und effiziente Methode zur Formylierung von Aryl- und Heteroarylbromiden Angewandte Chemie. 118: 161-165. DOI: 10.1002/Ange.200502697 |
0.449 |
|
| 2006 |
Mertins K, Iovel I, Kischel J, Zapf A, Beller M. Gold-catalyzed benzylation of arenes and heteroarenes Advanced Synthesis and Catalysis. 348: 691-695. DOI: 10.1002/Adsc.200505433 |
0.582 |
|
| 2005 |
Klaus S, Neumann H, Zapf A, Strübing D, Hübner S, Almena J, Riermeier T, Gross P, Sarich M, Krahnert WR, Rossen K, Beller M. A general and efficient method for the formylation of aryl and heteroaryl bromides. Angewandte Chemie (International Ed. in English). 45: 154-8. PMID 16304648 DOI: 10.1002/Anie.200502697 |
0.502 |
|
| 2005 |
Iovel I, Mertins K, Kischel J, Zapf A, Beller M. An efficient and general iron-catalyzed arylation of benzyl alcohols and benzyl carboxylates. Angewandte Chemie (International Ed. in English). 44: 3913-7. PMID 15900535 DOI: 10.1002/Anie.200462522 |
0.466 |
|
| 2005 |
Zapf A, Beller M. The development of efficient catalysts for palladium-catalyzed coupling reactions of aryl halides. Chemical Communications (Cambridge, England). 431-40. PMID 15654362 DOI: 10.1039/B410937F |
0.645 |
|
| 2005 |
Harkal S, Kumar K, Michalik D, Zapf A, Jackstell R, Rataboul F, Riermeier T, Monsees A, Beller M. An efficient catalyst system for diaryl ether synthesis from aryl chlorides Tetrahedron Letters. 46: 3237-3240. DOI: 10.1016/J.Tetlet.2005.03.033 |
0.795 |
|
| 2005 |
Schareina T, Zapf A, Beller M. An environmentally benign procedure for the Cu-catalyzed cyanation of aryl bromides Tetrahedron Letters. 46: 2585-2588. DOI: 10.1016/J.Tetlet.2005.02.106 |
0.554 |
|
| 2005 |
Tewari A, Hein M, Zapf A, Beller M. Efficient palladium catalysts for the amination of aryl chlorides: A comparative study on the use of phosphium salts as precursors to bulky, electron-rich phosphines Tetrahedron. 61: 9705-9709. DOI: 10.1016/J.Tet.2005.06.067 |
0.661 |
|
| 2005 |
Beller M, Zapf A, Riermeier T. CataCXium P Catalysts for Cross-Coupling Reactions of Aryl Halides Cheminform. 36. DOI: 10.1002/chin.200528236 |
0.437 |
|
| 2005 |
Iovel I, Mertins K, Kischel J, Zapf A, Beller M. Eine effiziente und allgemein anwendbare Fe-katalysierte Arylierung von Benzylalkoholen und Benzylcarboxylaten Angewandte Chemie. 117: 3981-3985. DOI: 10.1002/Ange.200462522 |
0.337 |
|
| 2004 |
Mertins K, Iovel I, Kischel J, Zapf A, Beller M. Transition-metal-catalyzed benzylation of arenes and heteroarenes. Angewandte Chemie (International Ed. in English). 44: 238-42. PMID 15614923 DOI: 10.1002/Anie.200460666 |
0.412 |
|
| 2004 |
Rataboul F, Zapf A, Jackstell R, Harkal S, Riermeier T, Monsees A, Dingerdissen U, Beller M. New ligands for a general palladium-catalyzed amination of aryl and heteroaryl chlorides. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 2983-90. PMID 15214081 DOI: 10.1002/Chem.200306026 |
0.777 |
|
| 2004 |
Schareina T, Zapf A, Beller M. Potassium hexacyanoferrate(II)--a new cyanating agent for the palladium-catalyzed cyanation of aryl halides. Chemical Communications (Cambridge, England). 1388-9. PMID 15179478 DOI: 10.1039/B400562G |
0.603 |
|
| 2004 |
Kumar K, Michalik D, Garcia Castro I, Tillack A, Zapf A, Arlt M, Heinrich T, Böttcher H, Beller M. Biologically active compounds through catalysis: efficient synthesis of N-(heteroarylcarbonyl)-N'-(arylalkyl)piperazines. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 746-57. PMID 14767940 DOI: 10.1002/Chem.200305327 |
0.603 |
|
| 2004 |
Zapf A, Jackstell R, Rataboul F, Riermeier T, Monsees A, Fuhrmann C, Shaikh N, Dingerdissen U, Beller M. Practical synthesis of new and highly efficient ligands for the Suzuki reaction of aryl chlorides. Chemical Communications (Cambridge, England). 38-9. PMID 14737321 DOI: 10.1039/B311268N |
0.774 |
|
| 2004 |
Kumar K, Zapf A, Michalik D, Tillack A, Heinrich T, Böttcher H, Arlt M, Beller M. Palladium-catalyzed carbonylation of haloindoles: no need for protecting groups. Organic Letters. 6: 7-10. PMID 14703337 DOI: 10.1021/Ol035988R |
0.616 |
|
| 2004 |
Tewari A, Hein M, Zapf A, Beller M. General synthesis and catalytic applications of di(1-adamantyl) alkylphosphines and their phosphonium salts Synthesis. 935-941. DOI: 10.1055/S-2004-822313 |
0.561 |
|
| 2004 |
Mertins K, Zapf A, Beller M. Catalytic borylation of o-xylene and heteroarenes via C-H activation Journal of Molecular Catalysis a: Chemical. 207: 21-25. DOI: 10.1016/S1381-1169(03)00470-9 |
0.585 |
|
| 2004 |
Tewari A, Hein M, Zapf A, Beller M. An easy three step synthesis of perfluoroalkylated amphetamines Tetrahedron Letters. 45: 7703-7707. DOI: 10.1016/J.Tetlet.2004.08.080 |
0.487 |
|
| 2004 |
Michalik D, Kumar K, Zapf A, Tillack A, Arlt M, Heinrich T, Beller M. A short and efficient synthesis of N-aryl- and N-heteroaryl-N′- (arylalkyl)piperazines Tetrahedron Letters. 45: 2057-2061. DOI: 10.1016/J.Tetlet.2004.01.066 |
0.53 |
|
| 2004 |
Frisch AC, Zapf A, Briel O, Kayser B, Shaikh N, Beller M. Comparison of palladium carbene and palladium phosphine catalysts for catalytic coupling reactions of aryl halides Journal of Molecular Catalysis a: Chemical. 214: 231-239. DOI: 10.1016/J.Molcata.2003.12.035 |
0.663 |
|
| 2004 |
Schareina T, Zapf A, Beller M. Improving palladium-catalyzed cyanation of aryl halides: Development of a state-of-the-art methodology using potassium hexacyanoferrate(II) as cyanating agent Journal of Organometallic Chemistry. 689: 4576-4583. DOI: 10.1016/J.Jorganchem.2004.08.020 |
0.6 |
|
| 2004 |
Kumar K, Michalik D, Garcia Castro I, Tillack A, Zapf A, Arlt M, Heinrich T, Böttcher H, Beller M. Cover Picture: Biologically Active Compounds through Catalysis: Efficient Synthesis ofN-(Heteroarylcarbonyl)-N′-(arylalkyl)piperazines (Chem. Eur. J. 3/2004) Chemistry - a European Journal. 10: 563-563. DOI: 10.1002/Chem.200490007 |
0.469 |
|
| 2004 |
Mertins K, Iovel I, Kischel J, Zapf A, Beller M. Übergangsmetallkatalysierte Benzylierung von Arenen und Heteroarenen Angewandte Chemie. 117: 242-246. DOI: 10.1002/Ange.200460666 |
0.353 |
|
| 2004 |
Harkal S, Rataboul F, Zapf A, Fuhrmann C, Riermeier T, Monsees A, Beller M. Dialkylphosphinoimidazoles as new ligands for palladium-catalyzed coupling reactions of aryl chlorides Advanced Synthesis and Catalysis. 346: 1742-1748. DOI: 10.1002/Adsc.200404213 |
0.797 |
|
| 2004 |
Schareina T, Zapf A, Beller M. Potassium hexacyanoferrate(II) - A new cyanating agent for the palladium-catalyzed cyanation of aryl halides Chemical Communications. 10: 1388-1389. |
0.306 |
|
| 2004 |
Beller M, Zapf A, Monsees A, Riermeier T. Cata CXium® P - Development and application of new efficient catalysts for cross-coupling reactions of aryl halides Chimica Oggi. 22: S16-S20. |
0.456 |
|
| 2003 |
Zapf A. Novel substrates for palladium-catalyzed coupling reactions of arenes. Angewandte Chemie (International Ed. in English). 42: 5394-9. PMID 14618571 DOI: 10.1002/Anie.200301681 |
0.508 |
|
| 2003 |
Sundermeier M, Zapf A, Beller M. A convenient procedure for the palladium-catalyzed cyanation of aryl halides. Angewandte Chemie (International Ed. in English). 42: 1661-4. PMID 12698471 DOI: 10.1002/Anie.200250778 |
0.573 |
|
| 2003 |
Sundermeier M, Zapf A, Mutyala S, Baumann W, Sans J, Weiss S, Beller M. Progress in the palladium-catalyzed cyanation of aryl chlorides. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 1828-36. PMID 12698441 DOI: 10.1002/Chem.200390210 |
0.646 |
|
| 2003 |
Frisch AC, Rataboul F, Zapf A, Beller M. First Kumada reaction of alkyl chlorides using N-heterocyclic carbene/palladium catalyst systems Journal of Organometallic Chemistry. 687: 403-409. DOI: 10.1016/S0022-328X(03)00723-X |
0.808 |
|
| 2003 |
Sundermeier M, Mutyala S, Zapf A, Spannenberg A, Beller M. A convenient and efficient procedure for the palladium-catalyzed cyanation of aryl halides using trimethylsilylcyanide Journal of Organometallic Chemistry. 684: 50-55. DOI: 10.1016/S0022-328X(03)00503-5 |
0.578 |
|
| 2003 |
Sundermeier M, Zapf A, Beller M. Palladium-Catalyzed Cyanation of Aryl Halides: Recent Developments and Perspectives European Journal of Inorganic Chemistry. 3513-3526. DOI: 10.1002/Ejic.200300162 |
0.616 |
|
| 2003 |
Sundermeier M, Zapf A, Beller M. Palladium-Catalyzed Cyanation of Aryl Halides: Recent Developments and Perspectives European Journal of Inorganic Chemistry. 2003: 3513-3526. DOI: 10.1002/EJIC.200300162 |
0.551 |
|
| 2003 |
Beller M, Zapf A. Palladium-Catalyzed Coupling Reactions for Industrial Fine Chemical Syntheses Cheminform. 34. DOI: 10.1002/CHIN.200335224 |
0.381 |
|
| 2003 |
Zapf A. Neue Substrate für Palladium-katalysierte Kupplungsreaktionen von Aromaten Angewandte Chemie. 115: 5552-5557. DOI: 10.1002/Ange.200301681 |
0.346 |
|
| 2003 |
Sundermeier M, Zapf A, Beller M. Ein praktikables Verfahren zur Palladium-katalysierten Cyanierung von Arylhalogeniden Angewandte Chemie. 115: 1700-1703. DOI: 10.1002/Ange.200250778 |
0.61 |
|
| 2002 |
Jackstell R, Gómez Andreu M, Frisch A, Selvakumar K, Zapf A, Klein H, Spannenberg A, Röttger D, Briel O, Karch R, Beller M. A highly efficient catalyst for the telomerization of 1,3-dienes with alcohols: first synthesis of a monocarbenepalladium(0)-olefin complex. Angewandte Chemie (International Ed. in English). 41: 986-9. PMID 12491289 DOI: 10.1002/1521-3773(20020315)41:6<986::Aid-Anie986>3.0.Co;2-M |
0.542 |
|
| 2002 |
Frisch AC, Shaikh N, Zapf A, Beller M. Palladium-catalyzed coupling of alkyl chlorides and grignard reagents. Angewandte Chemie (International Ed. in English). 41: 4056-9. PMID 12412080 DOI: 10.1002/1521-3773(20021104)41:21<4056::Aid-Anie4056>3.0.Co;2-8 |
0.611 |
|
| 2002 |
Selvakumar K, Zapf A, Spannenberg A, Beller M. Synthesis of monocarbenepalladium(0) complexes and their catalytic behavior in cross-coupling reactions of aryldiazonium salts. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 3901-6. PMID 12360931 DOI: 10.1002/1521-3765(20020902)8:17<3901::Aid-Chem3901>3.0.Co;2-E |
0.581 |
|
| 2002 |
Selvakumar K, Zapf A, Beller M. New palladium carbene catalysts for the Heck reaction of aryl chlorides in ionic liquids. Organic Letters. 4: 3031-3. PMID 12201709 DOI: 10.1021/ol020103h |
0.582 |
|
| 2002 |
Zapf A, Beller M. Topics in Catalysis. 19: 101-109. DOI: 10.1023/A:1013889401432 |
0.509 |
|
| 2002 |
Ehrentraut A, Zapf A, Beller M. A new improved catalyst for the palladium-catalyzed amination of aryl chlorides Journal of Molecular Catalysis a: Chemical. 182: 515-523. DOI: 10.1016/S1381-1169(01)00503-9 |
0.671 |
|
| 2002 |
Ehrentraut A, Zapf A, Beller M. Progress in the Palladium-Catalyzed α-Arylation of Ketones with Chloroarenes Advanced Synthesis and Catalysis. 344: 209-217. DOI: 10.1002/1615-4169(200202)344:2<209::Aid-Adsc209>3.0.Co;2-5 |
0.65 |
|
| 2002 |
Frisch AC, Shaikh N, Zapf A, Beller M. Palladium-katalysierte Kupplung von Alkylchloriden mit Grignard-Reagentien Angewandte Chemie. 114: 4218-4221. DOI: 10.1002/1521-3757(20021104)114:21<4218::Aid-Ange4218>3.0.Co;2-8 |
0.622 |
|
| 2002 |
Jackstell R, Gómez Andreu M, Frisch A, Selvakumar K, Zapf A, Klein H, Spannenberg A, Röttger D, Briel O, Karch R, Beller M. Ein hocheffizienter Katalysator für die Telomerisation von 1,3-Dienen mit Alkoholen: die erste Synthese eines Monocarbenolefinpalladium(0)-Komplexes Angewandte Chemie. 114: 1028-1031. DOI: 10.1002/1521-3757(20020315)114:6<1028::Aid-Ange1028>3.0.Co;2-# |
0.425 |
|
| 2001 |
Zapf A, Beller M. Palladium catalyst systems for cross-coupling reactions of aryl chlorides and olefins. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 2908-15. PMID 11486967 DOI: 10.1002/1521-3765(20010702)7:13<2908::Aid-Chem2908>3.0.Co;2-R |
0.667 |
|
| 2001 |
Sundermeier M, Zapf A, Beller M, Sans J. A new palladium catalyst system for the cyanation of aryl chlorides Tetrahedron Letters. 42: 6707-6710. DOI: 10.1016/S0040-4039(01)01390-9 |
0.648 |
|
| 2001 |
Gomez Andreu M, Zapf A, Beller M. ChemInform Abstract: Palladium-Catalyzed Synthesis of Fine Chemicals. Part 19. Molecularly Defined Palladium(0) Monophosphine Complexes as Catalysts for Efficient Cross-Coupling of Aryl Chlorides and Phenylboronic Acid. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200115105 |
0.498 |
|
| 2001 |
Zapf A, Ehrentraut A, Beller M. ChemInform Abstract: Palladium-Catalyzed Reactions for Fine Chemical Synthesis. Part 17. A New Highly Efficient Catalyst System for the Coupling of Nonactivated and Deactivated Aryl Chlorides with Arylboronic Acids. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200113104 |
0.63 |
|
| 2001 |
Ehrentraut A, Zapf A, Beller M. ChemInform Abstract: Palladium-Catalyzed Reactions for Fine Chemical Synthesis. Part 18. A New Efficient Palladium Catalyst for Heck Reactions of Deactivated Aryl Chlorides. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200108085 |
0.619 |
|
| 2001 |
Beller M, Zapf A. Efficient Synthesis of Fine Chemicals and Organic Building Blocks Applying Palladium-Catalyzed Coupling Reactions Chemie Ingenieur Technik. 73: 691-691. DOI: 10.1002/1522-2640(200106)73:6<691::Aid-Cite6914444>3.0.Co;2-X |
0.581 |
|
| 2001 |
Beller M, Zapf A, Mägerlein W. Efficient synthesis of fine chemicals and organic building blocks applying palladium-catalyzed coupling reactions Chemical Engineering and Technology. 24: 575-582. DOI: 10.1002/1521-4125(200106)24:6<575::Aid-Ceat575>3.0.Co;2-D |
0.643 |
|
| 2000 |
Zapf A, Ehrentraut A, Beller M. A New Highly Efficient Catalyst System for the Coupling of Nonactivated and Deactivated Aryl Chlorides with Arylboronic Acids Palladium-Catalyzed Reactions for Fine Chemical Synthesis, Part 17. The authors thank C. Fuhrmann for the excellent support in the laboratory, Dipl.-Chem. W. Mägerlein for ligand samples of 2-(dicyclohexylphosphanyl)toluene and -anisole as well as DMC(2) for generous donations of palladium compounds. Part 16: F. Vollmüller, W. Mägerlein, S. Klein, J. Krause, M. Beller, Adv. Synth. Catal., in press. Angewandte Chemie (International Ed. in English). 39: 4153-4155. PMID 11093237 DOI: 10.1002/1521-3773(20001117)39:22<4153::Aid-Anie4153>3.0.Co;2-T |
0.625 |
|
| 2000 |
Zapf A, Beller M. Palladium/phosphite catalyst systems for efficient cross coupling of aryl bromides and chlorides with phenylboronic acid Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 1830-3. PMID 10845642 DOI: 10.1002/(Sici)1521-3765(20000515)6:10<1830::Aid-Chem1830>3.0.Co;2-8 |
0.683 |
|
| 2000 |
Ehrentraut A, Zapf A, Beller M. A New Efficient Palladium Catalyst for Heck Reactions of Deactivated Aryl Chlorides Synlett. 2000: 1589-1592. DOI: 10.1055/S-2000-7919 |
0.651 |
|
| 2000 |
Andreu MG, Zapf A, Beller M. Molecularly defined palladium(0) monophosphine complexes as catalysts for efficient cross-coupling of aryl chlorides and phenylboronic acid1 Chemical Communications. 2475-2476. DOI: 10.1039/B006791L |
0.611 |
|
| 2000 |
Zapf A, Ehrentraut A, Beller M. Ein neues hocheffizientes Katalysatorsystem für die Kupplung von nichtaktivierten und desaktivierten Arylchloriden mit Arylboronsäuren Angewandte Chemie. 112: 4315-4317. DOI: 10.1002/1521-3757(20001117)112:22<4315::Aid-Ange4315>3.0.Co;2-L |
0.355 |
|
| 2000 |
Andreu MG, Zapf A, Beller M. Molecularly defined palladium(0) monophosphine complexes as catalysts for efficient cross-coupling of aryl chlorides and phenylboronic acid Chemical Communications. 2475-2476. |
0.434 |
|
| 2000 |
Ehrentraut A, Zapf A, Beller M. A new efficient palladium catalyst for Heck reactions of deactivated aryl chlorides Synlett. 1589-1592. |
0.502 |
|
| 1999 |
Beller M, Krauter JG, Zapf A, Bogdanovic S. Carbohydrate-substituted phosphines as new ligands for two-phase catalysis – synthesis and application Catalysis Today. 48: 279-290. DOI: 10.1016/S0920-5861(98)00383-6 |
0.598 |
|
| 1998 |
Beller M, Zapf A. Phosphites as Ligands for Efficient Catalysis of Heck Reactions Synlett. 1998: 792-793. DOI: 10.1055/S-1998-1760 |
0.579 |
|
| 1998 |
Beller M, Trauthwein H, Eichberger M, Breindl C, Müller TE, Zapf A. New cationic rhodium–amine complexes and their implication in the catalytic anti-Markovnikov oxidative amination of styrenes Journal of Organometallic Chemistry. 566: 277-285. DOI: 10.1016/S0022-328X(98)00745-1 |
0.547 |
|
| 1997 |
Beller M, Krauter JGE, Zapf A. Carbohydrate-Substituted Triarylphosphanes— A New Class of Ligands for Two-Phase Catalysis Angewandte Chemie International Edition in English. 36: 772-774. DOI: 10.1002/Anie.199707721 |
0.328 |
|
| 1997 |
Beller M, Krauter JGE, Zapf A. Kohlenhydratsutstituierte Triarylphosphane — eine neue Klasse von Liganden für die Zweiphasenkatalyse Angewandte Chemie. 109: 793-795. DOI: 10.1002/Ange.19971090726 |
0.34 |
|
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