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Wolfgang Dohle - Publications

Affiliations: 
1999-2002 Ludwig-Maximilians-Universität München, München, Bayern, Germany 
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34 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
2019 Dohle W, Su X, Mills SJ, Rossi AM, Taylor CW, Potter BVL. A synthetic cyclitol-nucleoside conjugate polyphosphate is a highly potent second messenger mimic. Chemical Science. 10: 5382-5390. PMID 31171961 DOI: 10.1039/C9Sc00445A  0.309
2018 Nel M, Joubert AM, Dohle W, Potter BV, Theron AE. Modes of cell death induced by tetrahydroisoquinoline-based analogs in MDA-MB-231 breast and A549 lung cancer cell lines. Drug Design, Development and Therapy. 12: 1881-1904. PMID 29983544 DOI: 10.2147/Dddt.S152718  0.383
2015 Shen YC, Upadhyayula R, Cevallos S, Messick RJ, Hsia T, Leese MP, Jewett DM, Ferrer-Torres D, Roth TM, Dohle W, Potter BV, Barald KF. Targeted NF1 cancer therapeutics with multiple modes of action: small molecule hormone-like agents resembling the natural anticancer metabolite, 2-methoxyoestradiol. British Journal of Cancer. 113: 1158-67. PMID 26461061 DOI: 10.1038/Bjc.2015.345  0.439
2014 Dohle W, Leese MP, Jourdan FL, Chapman CJ, Hamel E, Ferrandis E, Potter BV. Optimisation of tetrahydroisoquinoline-based chimeric microtubule disruptors. Chemmedchem. 9: 1783-93. PMID 24819406 DOI: 10.1002/Cmdc.201402025  0.48
2014 Leese MP, Jourdan FL, Major MR, Dohle W, Thomas MP, Hamel E, Ferrandis E, Mahon MF, Newman SP, Purohit A, Potter BV. Synthesis, anti-tubulin and antiproliferative SAR of steroidomimetic dihydroisoquinolinones. Chemmedchem. 9: 798-812. PMID 24596315 DOI: 10.1002/Cmdc.201400017  0.5
2014 Dohle W, Leese MP, Jourdan FL, Major MR, Bai R, Hamel E, Ferrandis E, Kasprzyk PG, Fiore A, Newman SP, Purohit A, Potter BV. Synthesis, antitubulin, and antiproliferative SAR of C3/C1-substituted tetrahydroisoquinolines. Chemmedchem. 9: 350-70. PMID 24436228 DOI: 10.1002/Cmdc.201300412  0.519
2014 Leese MP, Jourdan FL, Major MR, Dohle W, Hamel E, Ferrandis E, Fiore A, Kasprzyk PG, Potter BV. Tetrahydroisoquinolinone-based steroidomimetic and chimeric microtubule disruptors. Chemmedchem. 9: 85-108, 1. PMID 24124095 DOI: 10.1002/Cmdc.201300261  0.523
2012 Leese MP, Jourdan F, Dohle W, Kimberley MR, Thomas MP, Bai R, Hamel E, Ferrandis E, Potter BV. Steroidomimetic Tetrahydroisoquinolines for the Design of New Microtubule Disruptors. Acs Medicinal Chemistry Letters. 3: 5-9. PMID 22247790 DOI: 10.1021/Ml200232C  0.495
2011 Jourdan F, Leese MP, Dohle W, Ferrandis E, Newman SP, Chander S, Purohit A, Potter BV. Structure-activity relationships of C-17-substituted estratriene-3-O-sulfamates as anticancer agents. Journal of Medicinal Chemistry. 54: 4863-79. PMID 21604672 DOI: 10.1021/Jm200483X  0.523
2010 Jourdan F, Leese MP, Dohle W, Hamel E, Ferrandis E, Newman SP, Purohit A, Reed MJ, Potter BV. Synthesis, antitubulin, and antiproliferative SAR of analogues of 2-methoxyestradiol-3,17-O,O-bis-sulfamate. Journal of Medicinal Chemistry. 53: 2942-51. PMID 20225862 DOI: 10.1021/Jm9018806  0.526
2009 Lainchbury MD, Medley MI, Taylor PM, Hirst P, Dohle W, Booker-Milburn KI. Synthesis of ()-Neostenine Synfacts. 2009: 240-240. DOI: 10.1055/S-0028-1087693  0.409
2008 Lainchbury MD, Medley MI, Taylor PM, Hirst P, Dohle W, Booker-Milburn KI. A protecting group free synthesis of (+/-)-neostenine via the [5 + 2] photocycloaddition of maleimides. The Journal of Organic Chemistry. 73: 6497-505. PMID 18656978 DOI: 10.1021/Jo801108H  0.412
2006 Borthwick S, Dohle W, Hirst PR, Booker-Milburn KI. Copper-catalysed meso-bislactone ring opening using Grignard and mixed triorganozinc reagents Tetrahedron Letters. 47: 7205-7208. DOI: 10.1016/J.Tetlet.2006.07.146  0.395
2005 Hook BD, Dohle W, Hirst PR, Pickworth M, Berry MB, Booker-Milburn KI. A practical flow reactor for continuous organic photochemistry. The Journal of Organic Chemistry. 70: 7558-64. PMID 16149784 DOI: 10.1021/Jo050705P  0.313
2003 Dohle W, Staubitz A, Knochel P. Mild synthesis of polyfunctional benzimidazoles and indoles by the reduction of functionalized nitroarenes with phenylmagnesium chloride. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 5323-31. PMID 14613142 DOI: 10.1002/Chem.200305090  0.527
2003 Knochel P, Dohle W, Gommermann N, Kneisel FF, Kopp F, Korn T, Sapountzis I, Vu VA. Highly functionalized organomagnesium reagents prepared through halogen-metal exchange. Angewandte Chemie (International Ed. in English). 42: 4302-20. PMID 14502700 DOI: 10.1002/Anie.200300579  0.606
2003 Staubitz A, Dohle W, Knochel P. Expeditious Functionalization of Quinolines in Positions 2 and 8 via Polyfunctional Aryl- and Heteroarylmagnesium Intermediates Cheminform. 34. DOI: 10.1055/S-2003-36828  0.595
2003 Koradin C, Dohle W, Rodriguez AL, Schmid B, Knochel P. Synthesis of polyfunctional indoles and related heterocycles mediated by cesium and potassium bases Tetrahedron. 59: 1571-1587. DOI: 10.1016/S0040-4020(03)00073-5  0.787
2003 Knochel P, Dohle W, Gommermann N, Kneisel FF, Kopp F, Korn T, Sapountzis I, Vu VA. Synthese hoch funktionalisierter Organomagnesiumreagentien durch Halogen-Metall-Austausch Angewandte Chemie. 115: 4438-4456. DOI: 10.1002/Ange.200300579  0.376
2003 Staubitz A, Dohle W, Knochel P. Expeditious functionalization of quinolines in positions 2 and 8 via polyfunctional aryl- and heteroarylmagnesium intermediates Synthesis. 233-242.  0.321
2002 Lindsay DM, Dohle W, Jensen AE, Kopp F, Knochel P. Preparation of polyfunctional heterocycles using highly functionalized aminated arylmagnesium reagents as versatile scaffolds. Organic Letters. 4: 1819-22. PMID 12027622 DOI: 10.1021/Ol025597X  0.765
2002 Knochel P, Hupe E, Dohle W, Lindsay DM, Bonnet V, Quéguiner G, Boudier A, Kopp F, Demay S, Seidel N, Calaza MI, Vu VA, Sapountzis I, Bunlaksananusorn T. Functionalized main-group organometallics for organic synthesis Pure and Applied Chemistry. 74: 11-17. DOI: 10.1351/Pac200274010011  0.743
2002 Jensen AE, Dohle W, Sapountzis I, Lindsay DM, Vu VA, Knochel P. Preparation and Reactions of Functionalized Arylmagnesium Reagents Synthesis. 4: 565-569. DOI: 10.1055/S-2002-20955  0.732
2002 Knochel P, Hupe E, Dohle W, Lindsay DM, Bonnet V, Quéguiner G, Boudier A, Kopp F, Demay S, Seidel N, Calaza MI, Vu VA, Sapountzis I, Bunlaksananusorn T. Functionalized main-group organometallics for organic synthesis Pure and Applied Chemistry. 74: 11-17.  0.681
2002 Jensen AE, Dohle W, Sapountzis I, Lindsay DM, Vu VA, Knochel P. Preparation and reactions of functionalized arylmagnesium reagents Synthesis. 565-569.  0.737
2001 Sapountzis I, Dohle W, Knochel P. Stereoselective preparation of highly functionalized (Z)-3-magnesiated enoates by an iodine-magnesium exchange reaction. Chemical Communications (Cambridge, England). 2068-9. PMID 12240167 DOI: 10.1039/B106195J  0.541
2001 Dohle W, Lindsay DM, Knochel P. Copper-mediated cross-coupling of functionalized arylmagnesium reagents with functionalized alkyl and benzylic halides. Organic Letters. 3: 2871-3. PMID 11529778 DOI: 10.1021/Ol0163272  0.677
2001 Dohle W, Kopp F, Cahiez G, Knochel P. Fe(III)-Catalyzed Cross-Coupling Between Functionalized Arylmagnesium Compounds and Alkenyl Halides Synlett. 2001: 1901-1904. DOI: 10.1055/S-2001-18748  0.427
2001 Varchi G, Eeg Jensen A, Dohle W, Ricci A, Cahiez G, Knochel P. Preparation of Functionalized Magnesiated Aniline Derivatives Synlett. 2001: 0477-0480. DOI: 10.1055/S-2001-12323  0.52
2001 Varchi G, Jensen AE, Dohle W, Ricci A, Cahiez G, Knochel P. Preparation of functionalized magnesiated aniline derivatives Synlett. 477-480.  0.653
2000 Rodriguez AL, Koradin C, Dohle W, Knochel P. Versatile Indole Synthesis by a 5-endo-dig Cyclization Mediated by Potassium or Cesium Bases We thank the DFG (Leibniz-Programm) and the Fonds der Chemischen Industrie for generous financial support. A.L.R. and C. K. thank the Humboldt-Foundation and the BASF AG, respectively, for fellowships. W.D. was supported by the BMBF program (03 D 0056 2). We thank Dr. J. Henkelmann (BASF AG) for helpful discussions and the BASF AG for the generous gift of chemicals. Angewandte Chemie (International Ed. in English). 39: 2488-2490. PMID 10941112 DOI: 10.1002/1521-3773(20000717)39:14<2488::Aid-Anie2488>3.0.Co;2-E  0.717
2000 Jensen AE, Dohle W, Knochel P. Improved Nickel-Catalyzed Cross-Coupling Reaction Conditions between ortho -Substituted Aryl Iodides/Nonaflates and Alkylzinc Iodides in Solution and in the Solid-Phase Tetrahedron. 56: 4197-4201. DOI: 10.1016/S0040-4020(00)00344-6  0.704
2000 Rodriguez A, Koradin C, Dohle W, Knochel P. Vielseitige Indolsynthese durch eine Kalium- oder Caesiumbasen-vermittelte 5-endo-dig-Cyclisierung Angewandte Chemie. 112: 2607-2609. DOI: 10.1002/1521-3757(20000717)112:14<2607::Aid-Ange2607>3.0.Co;2-I  0.724
2000 Jensen AE, Dohle W, Knochel P. Improved nickel-catalyzed cross-coupling reaction conditions between ortho-substituted aryl iodides/nonaflates and alkylzinc iodides in solution and in the solid-phase Tetrahedron. 56: 4197-4201.  0.642
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