Year |
Citation |
Score |
2020 |
Mittendorf F, Mohr F, Kirsch SF. Ring Expansion of 2-Azido-2-phenyl-indan-1,3-dione for the Generation of Heterocyclic Scaffolds. The Journal of Organic Chemistry. 85: 12760-12769. PMID 32955884 DOI: 10.1021/Acs.Joc.0C01586 |
0.379 |
|
2020 |
Tong ML, Leusch LT, Holzschneider K, Kirsch SF. Rubazonic Acids and Their Synthesis. The Journal of Organic Chemistry. 85: 6008-6016. PMID 32293178 DOI: 10.1021/Acs.Joc.0C00465 |
0.407 |
|
2020 |
Ballaschk F, Özkaya Y, Kirsch SF. Stereocontrolled Synthesis of Harzialactone A and Its Three Stereoisomers by Use of Standardized Polyketide Building Blocks European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.202001046 |
0.344 |
|
2020 |
Borghi F, Çelik IE, Biallas P, Mittendorf F, Kirsch SF. Expanding the Versatile Reactivity of Diazido Malonic Acid Esters and Amides: Decarboxylation and Imine Formation European Journal of Organic Chemistry. 2020: 4389-4398. DOI: 10.1002/Ejoc.202000641 |
0.362 |
|
2019 |
Holzschneider K, Tong ML, Mohr F, Kirsch SF. A Synthetic Route Toward Tetrazoles: The Thermolysis of Geminal Diazides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31407837 DOI: 10.1002/Chem.201902131 |
0.432 |
|
2019 |
Biallas P, Mensak TM, Kunz KA, Kirsch SF. The Deazidoalkoxylation: Sequential Nucleophilic Substitutions with Diazidated Diethyl Malonate. The Journal of Organic Chemistry. 84: 1654-1663. PMID 30676025 DOI: 10.1021/Acs.Joc.8B02969 |
0.39 |
|
2019 |
Ottenbruch M, Mohr F, Kirsch SF. Synthesis of Sulfonylisoureas via Sulfo-Click Reactions Synthesis. 52: 695-702. DOI: 10.1055/S-0039-1691505 |
0.444 |
|
2019 |
Ballaschk F, Kirsch SF. Oxidation of secondary alcohols using solid-supported hypervalent iodine catalysts Green Chemistry. 21: 5896-5903. DOI: 10.1039/C9Gc02605C |
0.329 |
|
2019 |
Biallas P, Heider J, Kirsch SF. Functional polyamides withgem-diazido units: synthesis and diversification Polymer Chemistry. 10: 60-64. DOI: 10.1039/C8Py01087K |
0.316 |
|
2019 |
Holzschneider K, Häring AP, Kirsch SF. 2,2-Diazido-1,2-diarylethanones: Synthesis and Reactivity with Primary Amines European Journal of Organic Chemistry. 2019: 2824-2831. DOI: 10.1002/Ejoc.201900292 |
0.411 |
|
2018 |
Holzschneider K, Mohr F, Kirsch SF. Synthesis and Reactivity of 3,3-Diazidooxindoles. Organic Letters. PMID 30365325 DOI: 10.1021/Acs.Orglett.8B03013 |
0.444 |
|
2018 |
Holzschneider K, Kirsch SF. [1, 2]-Migration Reactions Catalyzed by Gold Complexes and their Applications in Total Synthesis Israel Journal of Chemistry. 58: 596-607. DOI: 10.1002/Ijch.201700081 |
0.432 |
|
2017 |
Holzschneider K, Häring AP, Haack A, Corey DJ, Benter T, Kirsch SF. Pathways in the Degradation of Geminal Diazides. The Journal of Organic Chemistry. PMID 28722411 DOI: 10.1021/Acs.Joc.7B01019 |
0.354 |
|
2017 |
Wagner C, Kotthaus AF, Kirsch SF. The asymmetric reduction of imidazolinones with trichlorosilane. Chemical Communications (Cambridge, England). PMID 28387397 DOI: 10.1039/C7Cc01561E |
0.465 |
|
2017 |
Biallas P, Häring AP, Kirsch SF. Cleavage of 1,3-dicarbonyls through oxidative amidation. Organic & Biomolecular Chemistry. PMID 28362452 DOI: 10.1039/C7Ob00731K |
0.404 |
|
2017 |
Tong ML, Huber F, Taghuo Kaptouom ES, Cellnik T, Kirsch SF. Enhanced site-selectivity in acylation reactions with substrate-optimized catalysts on solid supports. Chemical Communications (Cambridge, England). PMID 28243648 DOI: 10.1039/C7Cc00655A |
0.342 |
|
2017 |
Kirsch S, Kotthaus A, Ballaschk F, Stakaj V, Mohr F. Synthesis and Resolution of a Chiral Diamine: 2,2′-(Propane-2,2-diyl)dipyrrolidine Synthesis. 49: 3107-3111. DOI: 10.1055/S-0036-1589023 |
0.443 |
|
2017 |
Ballaschk F, Erhardt H, Kirsch SF. Synthesis of substituted pyrazines from N-allyl malonamides Rsc Advances. 7: 55594-55597. DOI: 10.1039/C7Ra11529F |
0.428 |
|
2017 |
Biallas P, Kirsch SF. Hydrogenolysis of geminal diazides Tetrahedron Letters. 58: 4209-4211. DOI: 10.1016/J.Tetlet.2017.09.066 |
0.406 |
|
2017 |
Häring AP, Biallas P, Kirsch SF. An Unconventional Reaction of 2,2-Diazido Acylacetates with Amines European Journal of Organic Chemistry. 2017: 1526-1539. DOI: 10.1002/Ejoc.201601625 |
0.394 |
|
2016 |
Erhardt H, Kunz KA, Kirsch SF. Thermolysis of Geminal Diazides: Reagent-Free Synthesis of 3-Hydroxypyridines. Organic Letters. PMID 27982590 DOI: 10.1021/Acs.Orglett.6B03475 |
0.476 |
|
2016 |
Huber F, Kirsch SF. Site-Selective Acylations with Tailor-Made Catalysts. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 5914-8. PMID 26970553 DOI: 10.1002/Chem.201600790 |
0.386 |
|
2016 |
Erhardt H, Mohr F, Kirsch SF. Synthesis of geminal bis- and tristriazoles: exploration of unconventional azide chemistry. Chemical Communications (Cambridge, England). 52: 545-8. PMID 26536826 DOI: 10.1039/C5Cc08163G |
0.434 |
|
2016 |
Erhardt H, Kirsch SF. Geminal Bis- and Tristriazoles: Long-known but still Uncommon Heterocyclic Entities Synthesis (Germany). 48: 1437-1456. DOI: 10.1055/S-0035-1560430 |
0.337 |
|
2016 |
Bredenkamp A, Zhu Z, Kirsch SF. A Chiral Building Block for the Stereocontrolled Installation of the 1,3-Diol Motif (Eur. J. Org. Chem. 2/2016) European Journal of Organic Chemistry. 2016. DOI: 10.1002/Ejoc.201690002 |
0.303 |
|
2016 |
Erhardt H, Mohr F, Kirsch SF. Synthesis of the 1,3,4-Oxadiazole Core through Thermolysis of Geminal Diazides European Journal of Organic Chemistry. 2016: 5629-5632. DOI: 10.1002/Ejoc.201601119 |
0.431 |
|
2015 |
Bredenkamp A, Wegener M, Hummel S, Häring AP, Kirsch SF. Versatile process for the stereodiverse construction of 1,3-polyols: iterative chain elongation with chiral building blocks. Chemical Communications (Cambridge, England). PMID 26673147 DOI: 10.1039/C5Cc09328G |
0.313 |
|
2015 |
Erhardt H, Häring AP, Kotthaus A, Roggel M, Tong ML, Biallas P, Jübermann M, Mohr F, Kirsch SF. Geminal Diazides Derived from 1,3-Dicarbonyls: A Protocol for Synthesis. The Journal of Organic Chemistry. PMID 26623662 DOI: 10.1021/Acs.Joc.5B02328 |
0.433 |
|
2015 |
Häring AP, Kirsch SF. Synthesis and Chemistry of Organic Geminal Di- and Triazides. Molecules (Basel, Switzerland). 20: 20042-62. PMID 26561796 DOI: 10.3390/Molecules201119675 |
0.368 |
|
2015 |
Wegener M, Kirsch SF. The reactivity of 4-hydroxy- and 4-silyloxy-1,5-allenynes with homogeneous gold(I) catalysts. Organic Letters. 17: 1465-8. PMID 25739001 DOI: 10.1021/Acs.Orglett.5B00348 |
0.468 |
|
2015 |
Wegener M, Huber F, Bolli C, Jenne C, Kirsch SF. Silver-free activation of ligated gold(I) chlorides: the use of [Me3NB12Cl11]- as a weakly coordinating anion in homogeneous gold catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 1328-36. PMID 25394284 DOI: 10.1002/Chem.201404487 |
0.362 |
|
2015 |
Kirsch S, Bredenkamp A, Mohr F. Synthesis of Isatins through Direct Oxidation of Indoles with IBX-SO3K/NaI Synthesis. 47: 1937-1943. DOI: 10.1055/S-0034-1380517 |
0.342 |
|
2015 |
Häring AP, Kirsch SF. Propargyl Vinyl Ethers as Powerful Starting Points for Heterocycle Synthesis Progress in Heterocyclic Chemistry. 27: 1-28. DOI: 10.1016/B978-0-08-100024-3.00001-5 |
0.367 |
|
2015 |
Bredenkamp A, Zhu Z, Kirsch SF. A Chiral Building Block for the Stereocontrolled Installation of the 1,3-Diol Motif European Journal of Organic Chemistry. 2016: 252-254. DOI: 10.1002/Ejoc.201501325 |
0.393 |
|
2015 |
Haering AP, Klahn P, Juebermann M, Mohr F, Kirsch SF. ChemInform Abstract: Gold(I)-Catalyzed Heterocyclization of β-Alkynyl Hydroxamic Acids: Synthesis of Isoxazolidin-3-ones. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201521154 |
0.719 |
|
2015 |
Palisse A, Kirsch SF. ChemInform Abstract: Synthesis of Furans Through Silver-Catalyzed Propargyl-Claisen Rearrangement Followed by Cyclocondensation. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201516145 |
0.381 |
|
2015 |
Klahn P, Kirsch SF. ChemInform Abstract: IBX-Mediated Dehydrogenation of Substituted β-Oxonitriles. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201506179 |
0.668 |
|
2014 |
Klahn P, Erhardt H, Kotthaus A, Kirsch SF. The synthesis of α-azidoesters and geminal triazides. Angewandte Chemie (International Ed. in English). 53: 7913-7. PMID 24895221 DOI: 10.1002/Anie.201402433 |
0.744 |
|
2014 |
Umland KD, Mayer C, Kirsch SF. Oxidative Chlorination of Activated Methylene Compounds with Sodium Chloride Synlett. 25: 813-816. DOI: 10.1055/S-0033-1340793 |
0.394 |
|
2014 |
Häring AP, Klahn P, Jübermann M, Mohr F, Kirsch SF. Gold(I)-catalyzed heterocyclization of β-alkynyl hydroxamic acids: synthesis of isoxazolidin-3-ones Monatshefte FüR Chemie - Chemical Monthly. 146: 119-134. DOI: 10.1007/S00706-014-1319-1 |
0.738 |
|
2014 |
Palisse A, Kirsch SF. Synthesis of furans through silver-catalyzed propargyl-claisen rearrangement followed by cyclocondensation European Journal of Organic Chemistry. 2014: 7095-7098. DOI: 10.1002/Ejoc.201402983 |
0.479 |
|
2014 |
Klahn P, Kirsch SF. IBX-mediated dehydrogenation of substituted β-oxonitriles European Journal of Organic Chemistry. 2014: 3149-3155. DOI: 10.1002/Ejoc.201402007 |
0.727 |
|
2014 |
Klahn P, Erhardt H, Kotthaus A, Kirsch SF. Über die Synthese von α-Azidoestern und geminalen Triaziden Angewandte Chemie. 126: 8047-8051. DOI: 10.1002/Ange.201402433 |
0.667 |
|
2013 |
Huber F, Kirsch SF. NIS-mediated electrophilic cyclization of 3-silyloxy-1,n-enynes. The Journal of Organic Chemistry. 78: 2780-5. PMID 23410107 DOI: 10.1021/Jo302751P |
0.308 |
|
2013 |
Zhu ZB, Kirsch SF. Propargyl vinyl ethers as heteroatom-tethered enyne surrogates: diversity-oriented strategies for heterocycle synthesis. Chemical Communications (Cambridge, England). 49: 2272-83. PMID 23340491 DOI: 10.1039/C3Cc37258H |
0.408 |
|
2013 |
Umland KD, Kirsch SF. When alkyne π-activation meets pinacol-type [1,2]-rearrangement: On the invention of domino reactions for the synthesis of carbocycles and heterocycles Synlett. 24: 1471-1484. DOI: 10.1055/S-0033-1338840 |
0.437 |
|
2013 |
Umland K, Kirsch SF. ChemInform Abstract: When Alkyne π-Activation Meets Pinacol-Type [1,2]-Rearrangement: On the Invention of Domino Reactions for the Synthesis of Carbocycles and Heterocycles Cheminform. 44: no-no. DOI: 10.1002/CHIN.201339253 |
0.342 |
|
2012 |
Palisse A, Kirsch SF. Metal-free reactions of alkynes via electrophilic iodocarbocyclizations. Organic & Biomolecular Chemistry. 10: 8041-7. PMID 22987122 DOI: 10.1039/C2Ob26508G |
0.369 |
|
2012 |
Klahn P, Duschek A, Liébert C, Kirsch SF. Total synthesis of (+)-cyperolone. Organic Letters. 14: 1250-3. PMID 22324453 DOI: 10.1021/Ol300058T |
0.736 |
|
2012 |
Harschneck T, Hummel S, Kirsch SF, Klahn P. Practical azidation of 1,3-dicarbonyls. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 1187-93. PMID 22189938 DOI: 10.1002/Chem.201102680 |
0.727 |
|
2011 |
Umland KD, Palisse A, Haug TT, Kirsch SF. Domino reactions consisting of heterocyclization and 1,2-migration-redox-neutral and oxidative transition-metal catalysis. Angewandte Chemie (International Ed. in English). 50: 9965-8. PMID 21898734 DOI: 10.1002/Anie.201103961 |
0.386 |
|
2011 |
Hummel S, Kirsch SF. When gold can do what iodine cannot do: A critical comparison. Beilstein Journal of Organic Chemistry. 7: 847-59. PMID 21804881 DOI: 10.3762/Bjoc.7.97 |
0.408 |
|
2011 |
Harschneck T, Kirsch SF. One-pot synthesis of 1,2-dihydropyridines: expanding the diverse reactivity of propargyl vinyl ethers. The Journal of Organic Chemistry. 76: 2145-56. PMID 21381702 DOI: 10.1021/Jo102545M |
0.493 |
|
2011 |
Duschek A, Kirsch SF. 2-Iodoxybenzoic acid--a simple oxidant with a dazzling array of potential applications. Angewandte Chemie (International Ed. in English). 50: 1524-52. PMID 21271626 DOI: 10.1002/Anie.201000873 |
0.313 |
|
2011 |
Kirsch S, Klahn P, Menz H. The Use of COP-OAc in the Catalyst-Controlled Syntheses of 1,3-Polyols Synthesis. 2011: 3592-3603. DOI: 10.1055/S-0031-1289574 |
0.697 |
|
2011 |
Harschneck T, Kirsch SF, Wegener M. Electrophilic Cyclization of 1,6-Enynes Synlett. 2011: 1151-1153. DOI: 10.1055/S-0030-1259938 |
0.375 |
|
2011 |
Harschneck T, Kirsch SF, Wegener M. ChemInform Abstract: Electrophilic Cyclization of 1,6-Enynes. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201138032 |
0.304 |
|
2011 |
Cannon JS, Kirsch SF, Overman LE. ChemInform Abstract: Catalytic Asymmetric Synthesis of Chiral Allylic Esters. Cheminform. 42: no-no. DOI: 10.1002/chin.201112045 |
0.736 |
|
2011 |
Klahn P, Kirsch SF. Electronic Fine-Tuning of Carbene Ligands and its Impact on Gold Catalysis Chemcatchem. 3: 649-652. DOI: 10.1002/Cctc.201000366 |
0.664 |
|
2010 |
Cannon JS, Kirsch SF, Overman LE, Sneddon HF. Mechanism of the cobalt oxazoline palladacycle (COP)-catalyzed asymmetric synthesis of allylic esters. Journal of the American Chemical Society. 132: 15192-203. PMID 20942424 DOI: 10.1021/Ja106688J |
0.741 |
|
2010 |
Cannon JS, Kirsch SF, Overman LE. Catalytic asymmetric synthesis of chiral allylic esters. Journal of the American Chemical Society. 132: 15185-91. PMID 20942420 DOI: 10.1055/S-2005-869916 |
0.754 |
|
2010 |
Crone B, Kirsch SF, Umland KD. Electrophilic cyclization of 1,5-enynes. Angewandte Chemie (International Ed. in English). 49: 4661-4. PMID 20480473 DOI: 10.1002/Anie.201001113 |
0.352 |
|
2010 |
Haug TT, Kirsch SF. Total synthesis of (+)-chloriolide Organic and Biomolecular Chemistry. 8: 991-993. PMID 20165786 DOI: 10.1039/B925644J |
0.391 |
|
2010 |
Menz H, Kirsch SF. Synthesis of Polyrhacitides A and B Synfacts. 2010: 504-504. DOI: 10.1055/S-0029-1219710 |
0.323 |
|
2010 |
Bach T, Kirsch S. ChemInform Abstract: Synthesis of 6-Substituted 4-Hydroxy-2-pyrones from Aldehydes by Addition of an Acetoacetate Equivalent, Dess-Martin Oxidation and Subsequent Cyclization. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200215140 |
0.337 |
|
2009 |
Menz H, Kirsch SF. Total synthesis of polyrhacitides A and B by Use of an iterative strategy for the stereoselective synthesis of 1,3-Polyol arrays Organic Letters. 11: 5634-5637. PMID 19919037 DOI: 10.1021/Ol902135V |
0.36 |
|
2009 |
Kirsch S, Lange A, Heydenreuter W, Menz H. Transition-Metal-Catalyzed Rearrangement of 1,1-(Oligomethylene)-4-aryl-2-butene-1,4-diols: Ring Expansion vs. Aryl Group Migration Synlett. 2009: 2987-2991. DOI: 10.1055/S-0029-1218274 |
0.35 |
|
2009 |
Menz H, Binder JT, Crone B, Duschek A, Haug TT, Kirsch SF, Klahn P, Liébert C. Gold-catalyzed reactivity of 3-silyloxy-1,5-enynes: a synthetic tool for the synthesis of complex structures and its limitations Tetrahedron. 65: 1880-1888. DOI: 10.1016/J.Tet.2008.11.103 |
0.755 |
|
2009 |
Haug TT, Harschneck T, Duschek A, Lee C, Binder JT, Menz H, Kirsch SF. Reactivity of 3-silyloxy-1,4-enynes: Gold(III)-catalyzed regioselective nucleophilic substitution Journal of Organometallic Chemistry. 694: 510-514. DOI: 10.1016/J.Jorganchem.2008.09.062 |
0.474 |
|
2009 |
Haug TT, Harschneck T, Duschek A, Lee C, Binder JT, Menz H, Kirsch SF. ChemInform Abstract: Reactivity of 3-Silyloxy-1,4-enynes: Gold(III)-Catalyzed Regioselective Nucleophilic Substitution. Cheminform. 40. DOI: 10.1002/CHIN.200927053 |
0.341 |
|
2009 |
Menz H, Binder JT, Crone B, Duschek A, Haug TT, Kirsch SF, Klahn P, Liebert C. ChemInform Abstract: Gold-Catalyzed Reactivity of 3-Silyloxy-1,5-enynes: A Synthetic Tool for the Synthesis of Complex Structures and Its Limitations. Cheminform. 40. DOI: 10.1002/CHIN.200927028 |
0.716 |
|
2008 |
Baskar B, Bae HJ, An SE, Cheong JY, Rhee YH, Duschek A, Kirsch SF. Gold(I)-catalyzed divergence in the reactivity of 3-silyloxy 1,6-enynes: pinacol-terminated vs claisen-terminated cyclization cascades. Organic Letters. 10: 2605-7. PMID 18476705 DOI: 10.1021/Ol8008733 |
0.609 |
|
2008 |
Crone B, Kirsch SF. 1,2-Alkyl migration as a key element in the invention of cascade reactions catalyzed by pi-acids. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 3514-22. PMID 18318026 DOI: 10.1002/Chem.200701985 |
0.436 |
|
2008 |
Binder JT, Crone B, Haug TT, Menz H, Kirsch SF. Direct carbocyclization of aldehydes with alkynes: combining gold catalysis with aminocatalysis. Organic Letters. 10: 1025-8. PMID 18232707 DOI: 10.1021/Ol800092P |
0.403 |
|
2008 |
Kirsch SF. Construction of heterocycles by the strategic use of alkyne π-activation in catalyzed cascade reactions Synthesis. 3183-3204. DOI: 10.1055/S-0028-1083164 |
0.483 |
|
2008 |
Crone B, Kirsch SF. 1,2-Alkyl migration as a key element in the invention of cascade reactions catalyzed by π-acids Chemistry - a European Journal. 14: 3514-3522. DOI: 10.1002/chem.200701985 |
0.345 |
|
2008 |
Duschek A, Kirsch SF. Combining the concepts: Dual Catalysis with carbophilic Lewis acids Angewandte Chemie - International Edition. 47: 5703-5705. DOI: 10.1002/anie.200801903 |
0.352 |
|
2007 |
Binder JT, Kirsch SF. Iterative approach to polyketide-type structures: Stereoselective synthesis of 1,3-polyols utilizing the catalytic asymmetric Overman esterification Chemical Communications. 4164-4166. PMID 17925963 DOI: 10.1039/B708248G |
0.405 |
|
2007 |
Crone B, Kirsch SF. Synthesis of 4-iodo-3-furanones utilizing electrophile-induced tandem cyclization/1,2-migration reactions Journal of Organic Chemistry. 72: 5435-5438. PMID 17555360 DOI: 10.1021/Jo070695N |
0.439 |
|
2007 |
Kirsch SF, Binder JT, Crone B, Duschek A, Haug TT, Liébert C, Menz H. Catalyzed tandem reaction of 3-silyloxy-1,5-enynes consisting of cyclization and pinacol rearrangement. Angewandte Chemie (International Ed. in English). 46: 2310-3. PMID 17310486 DOI: 10.1002/Anie.200604544 |
0.419 |
|
2007 |
Kirsch SF, Overman LE, White NS. Catalytic asymmetric synthesis of allylic aryl ethers. Organic Letters. 9: 911-3. PMID 17274626 DOI: 10.1021/Ol070110B |
0.723 |
|
2007 |
Kirsch SF, Liebert C. Neodymium(III)-Mediated Reformatsky-Type Reactions of α-Halo Ketones with Carbonyl Compounds. Cheminform. 38. DOI: 10.1002/Ejoc.200700240 |
0.435 |
|
2007 |
Kirsch SF, Liébert C. Neodymium(III)-mediated reformatsky-type reactions of α-halo ketones with carbonyl compounds European Journal of Organic Chemistry. 3711-3717. DOI: 10.1002/ejoc.200700240 |
0.327 |
|
2007 |
Binder JT, Crone B, Kirsch SF, Liébert C, Menz H. Synthesis of Heterocyclic Systems by Transition-Metal-Catalyzed Cyclization-Migration Reactions – A Diversity-Oriented Strategy for the Construction of Spirocyclic 3(2H)-Furanones and 3-Pyrrolones European Journal of Organic Chemistry. 2007: 1636-1647. DOI: 10.1002/Ejoc.200601060 |
0.488 |
|
2007 |
Anderson CE, Kirsch SF, Overman LE, Richards CJ, Watson MP. Preparation of the cop catalysts: [(S)-COP-OAc]2, [(S)-COP-Cl]2, and (S)-COP-hfacac Organic Syntheses. 84: 148-155. DOI: 10.1002/0471264229.Os084.15 |
0.731 |
|
2006 |
Menz H, Kirsch SF. Synthesis of stable 2H-pyran-5-carboxylates via a catalyzed propargyl-Claisen rearrangement/oxa-6pi electrocyclization strategy. Organic Letters. 8: 4795-7. PMID 17020305 DOI: 10.1021/Ol061856X |
0.443 |
|
2006 |
Kirsch SF, Binder JT, Liébert C, Menz H. Gold(III)- and platinum(II)-catalyzed domino reaction consisting of heterocyclization and 1,2-migration: efficient synthesis of highly substituted 3(2H)-furanones. Angewandte Chemie (International Ed. in English). 45: 5878-80. PMID 16871607 DOI: 10.1002/Anie.200601836 |
0.421 |
|
2006 |
Kirsch SF. Syntheses of polysubstituted furans: Recent developments Organic and Biomolecular Chemistry. 4: 2076-2080. PMID 16729118 DOI: 10.1039/B602596J |
0.364 |
|
2006 |
Binder JT, Kirsch SF. Synthesis of highly substituted pyrroles via a multimetal-catalyzed rearrangement-condensation-cyclization domino approach. Organic Letters. 8: 2151-3. PMID 16671804 DOI: 10.1021/Ol060664Z |
0.486 |
|
2006 |
Crone B, Kirsch SF. A new method for the synthesis of Z-enediones via IBX-mediated oxidative rearrangement of 2-alkynyl alcohol systems. Chemical Communications (Cambridge, England). 764-6. PMID 16465333 DOI: 10.1039/B515838A |
0.343 |
|
2006 |
Menz H, Kirsch SF. Synthesis of stable 2H-pyran-5-carboxylates via a catalyzed propargyl-claisen rearrangement/oxa-6π electrocyclization strategy Organic Letters. 8: 4795-4797. DOI: 10.1021/ol061856x |
0.315 |
|
2006 |
Binder JT, Kirsch SF. Synthesis of highly substituted pyrroles via a multimetal-catalyzed rearrangement-condensation-cyclization domino approach Organic Letters. 8: 2151-2153. DOI: 10.1021/ol060664z |
0.375 |
|
2005 |
Kirsch SF. IBX-mediated alpha-hydroxylation of alpha-alkynyl carbonyl systems. A convenient method for the synthesis of tertiary alcohols. The Journal of Organic Chemistry. 70: 10210-2. PMID 16292876 DOI: 10.1021/Jo051898J |
0.32 |
|
2005 |
Kirsch SF, Bach T. Diastereoselective reactions at enantiomerically pure, sterically congested cyclohexanes as an entry to wailupemycins A and B: Total synthesis of (+)-wailupemycin B Chemistry - a European Journal. 11: 7007-7023. PMID 16144024 DOI: 10.1002/Chem.200500640 |
0.588 |
|
2005 |
Suhre MH, Reif M, Kirsch SF. Gold(I)-catalyzed synthesis of highly substituted furans. Organic Letters. 7: 3925-7. PMID 16119933 DOI: 10.1021/Ol0514101 |
0.52 |
|
2005 |
Kirsch SF, Overman LE. Catalytic asymmetric intramolecular aminopalladation: improved palladium(II) catalysts. The Journal of Organic Chemistry. 70: 2859-61. PMID 15787588 DOI: 10.1021/Jo047763F |
0.565 |
|
2005 |
Kirsch SF, Overman LE. Catalytic asymmetric synthesis of chiral allylic esters. Journal of the American Chemical Society. 127: 2866-7. PMID 15740118 DOI: 10.1021/Ja0425583 |
0.59 |
|
2005 |
Kirsch SF, Bach T. Chiral 2,4,6-trihydroxycyclohexanones as potent building blocks: A convenient method for the preparation of enantiomerically pure acyclic 1,3-diols Synthesis. 2657-2660. DOI: 10.1055/S-2005-872141 |
0.577 |
|
2004 |
Kirsch SF, Overman LE, Watson MP. Monomeric cobalt oxazoline palladacycles (COP). Useful catalysts for catalytic asymmetric rearrangement of allylic trichloroacetimidates. The Journal of Organic Chemistry. 69: 8101-4. PMID 15527296 DOI: 10.1021/Jo0487092 |
0.708 |
|
2004 |
Kirsch S, Ackermann O, Harms K, Bach T. Regioselective Isomerization of Highly Substituted 1-Methylenecyclohexenepoxides to the Corresponding Allylic Alcohols. Influence of the Base and of the Protecting Groups. Cheminform. 35. DOI: 10.1007/S00706-003-0153-7 |
0.534 |
|
2003 |
Kirsch S, Bach T. Total synthesis of (+)-wailupemycin B Angewandte Chemie - International Edition. 42: 4685-4687. PMID 14533164 DOI: 10.1002/Anie.200351455 |
0.556 |
|
2003 |
Kirsch S, Bach T. Stereoselective Synthesis ofEnantiomerically Pure, Orthogonally Protected 2-Methylenecyclohexane-1,3,5-triolsand 2,4,6-Trihydroxycyclohexanones Synthesis. 2003: 1827-1836. DOI: 10.1055/S-2003-41025 |
0.514 |
|
2003 |
Kirsch S, Bach T. Totalsynthese von (+)-Wailupemycin B Angewandte Chemie. 115: 4833-4835. DOI: 10.1002/Ange.200351455 |
0.41 |
|
2001 |
Bach T, Kirsch S. Synthesis of 6-Substituted 4-Hydroxy-2-pyrones from Aldehydes by Addition of an Acetoacetate Equivalent, Dess-Martin Oxidation and Subsequent Cyclization Synlett. 2001: 1974-1976. DOI: 10.1055/S-2001-18759 |
0.583 |
|
Low-probability matches (unlikely to be authored by this person) |
2023 |
Mittendorf F, Quambusch M, Kirsch SF. Total synthesis of both enantiomers of the biosurfactant aureosurfactin bidirectional synthesis with a chiral Horner-Wittig building block. Organic & Biomolecular Chemistry. 21: 4574-4577. PMID 37222559 DOI: 10.1039/d3ob00650f |
0.295 |
|
2009 |
Kirsch SF. ChemInform Abstract: Construction of Heterocycles by the Strategic Use of Alkyne π-Activation in Catalyzed Cascade Reactions Cheminform. 40. DOI: 10.1002/CHIN.200903242 |
0.288 |
|
2008 |
Duschek A, Kirsch SF. Combining the concepts: dual catalysis with carbophilic Lewis acids. Angewandte Chemie (International Ed. in English). 47: 5703-5. PMID 18613157 DOI: 10.1002/Anie.200801903 |
0.287 |
|
2009 |
Kirsch S. Fundamentals of Asymmetric Catalysis.Von Patrick J. Walsh und Marisa C. Kozlowski. Angewandte Chemie. 121: 2486-2487. DOI: 10.1002/Ange.200900669 |
0.276 |
|
2010 |
Harschneck T, Kirsch SF. Quickly to biaryls: Direct arylation with aryl halogenoids Nachrichten Aus Der Chemie. 58: 544-547. DOI: 10.1002/Nadc.201073883 |
0.273 |
|
2020 |
Wolf J, Huber F, Erochok N, Heinen F, Guerin V, Legault C, Kirsch S, Huber SM. Activation of a metal-halogen bond by halogen bonding. Angewandte Chemie (International Ed. in English). PMID 32472957 DOI: 10.1002/Anie.202005214 |
0.273 |
|
2009 |
Kirsch S. Fundamentals of Asymmetric Catalysis.By Patrick J. Walsh and Marisa C. Kozlowski. Angewandte Chemie International Edition. 48: 2450-2451. DOI: 10.1002/Anie.200900669 |
0.27 |
|
2010 |
Menz H, Kirsch SF. ChemInform Abstract: Total Synthesis of Polyrhacitides A (I) and B (II) by Use of an Iterative Strategy for the Stereoselective Synthesis of 1,3-Polyol Arrays. Cheminform. 41. DOI: 10.1002/CHIN.201019198 |
0.265 |
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2009 |
Duschek A, Kirsch SF. Novel oxygenations with IBX Chemistry - a European Journal. 15: 10713-10717. DOI: 10.1002/chem.200901867 |
0.262 |
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2022 |
Mittendorf F, Celik IE, Kirsch SF. Total Synthesis of Cryptoconcatone D via Construction of 1,3-Diol Units Using Chiral Horner-Wittig Reagents. The Journal of Organic Chemistry. PMID 36195315 DOI: 10.1021/acs.joc.2c01737 |
0.259 |
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2011 |
Kummerlöwe G, Crone B, Kretschmer M, Kirsch SF, Luy B. Back Cover: Residual Dipolar Couplings as a Powerful Tool for Constitutional Analysis: The Unexpected Formation of Tricyclic Compounds (Angew. Chem. Int. Ed. 11/2011) Angewandte Chemie International Edition. 50: 2648-2648. DOI: 10.1002/Anie.201101025 |
0.258 |
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2006 |
Kirsch SF, Binder JT, Liébert C, Menz H. Gold(III)- und Platin(II)-katalysierte Dominoreaktion aus Heterocyclisierung und 1,2-Verschiebung: effiziente Synthese von hoch substituierten 3(2H)-Furanonen Angewandte Chemie. 118: 6010-6013. DOI: 10.1002/Ange.200601836 |
0.256 |
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2011 |
Kummerlöwe G, Crone B, Kretschmer M, Kirsch SF, Luy B. Residual dipolar couplings as a powerful tool for constitutional analysis: the unexpected formation of tricyclic compounds. Angewandte Chemie (International Ed. in English). 50: 2643-5. PMID 21370357 DOI: 10.1002/Anie.201007305 |
0.256 |
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2011 |
Duschek A, Kirsch SF. 2-Iodoxybenzoesäure - ein einfaches Oxidationsmittel mit einer Vielfalt an Anwendungsmöglichkeiten Angewandte Chemie. 123: 1562-1590. DOI: 10.1002/Ange.201000873 |
0.251 |
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2012 |
Nodwell MB, Menz H, Kirsch SF, Sieber SA. Rugulactone and its analogues exert antibacterial effects through multiple mechanisms including inhibition of thiamine biosynthesis. Chembiochem : a European Journal of Chemical Biology. 13: 1439-46. PMID 22653914 DOI: 10.1002/Cbic.201200265 |
0.251 |
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2015 |
Bredenkamp A, Mohr F, Kirsch SF. ChemInform Abstract: Synthesis of Isatins Through Direct Oxidation of Indoles with IBX-SO3K/NaI. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201549107 |
0.25 |
|
2006 |
Kirsch SF, Bach T. Chiral 2,4,6-Trihydroxycyclohexanones as Potent Building Blocks: A Convenient Method for the Preparation of Enantiomerically Pure Acyclic 1,3-Diols. Cheminform. 37. DOI: 10.1002/chin.200608054 |
0.248 |
|
2006 |
Crone B, Kirsch SF. A new method for the synthesis of Z-enediones via IBX-mediated oxidative rearrangement of 2-alkynyl alcohol systems Chemical Communications. 764-766. DOI: 10.1039/b515838a |
0.248 |
|
2005 |
Kirsch SF. IBX-mediated α-hydroxylation of α-alkynyl carbonyl systems. A convenient method for the synthesis of tertiary alcohols Journal of Organic Chemistry. 70: 10210-10212. DOI: 10.1021/jo051898j |
0.245 |
|
2011 |
Umland K, Palisse A, Haug TT, Kirsch SF. Dominoreaktionen bestehend aus Heterocyclisierung und 1,2-Verschiebung - redoxneutrale und oxidative Übergangsmetallkatalyse im Vergleich Angewandte Chemie. 123: 10140-10143. DOI: 10.1002/Ange.201103961 |
0.237 |
|
2015 |
Wegener M, Kirsch SF. The reactivity of 4-hydroxy- and 4-silyloxy-1,5-allenynes with homogeneous gold(I) catalysts Organic Letters. 17: 1465-1468. DOI: 10.1021/acs.orglett.5b00348 |
0.235 |
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2010 |
Kirsch S, Harschneck T. Elegant und nützlich: Biomimetische Synthesestrategien Nachrichten Aus Der Chemie. 58: 1131-1135. DOI: 10.1002/Nadc.201076782 |
0.234 |
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2010 |
Harschneck T, Kirsch SF. ChemInform Abstract: A Rapid Approach to Biaryls: Direct Arylation with Aryl Halides Cheminform. 41: no-no. DOI: 10.1002/CHIN.201029254 |
0.234 |
|
2007 |
Kirsch S, Binder J, Crone B, Duschek A, Haug T, Liébert C, Menz H. Katalysierte Tandemreaktion aus Cyclisierung und Pinakol-Umlagerung von 3-Silyloxy-1,5-eninen Angewandte Chemie. 119: 2360-2363. DOI: 10.1002/Ange.200604544 |
0.23 |
|
2007 |
Binder JT, Crone B, Kirsch SF, Liebert C, Menz H. Synthesis of Heterocyclic Systems by Transition Metal Catalyzed Cyclization—Migration Reactions — A Diversity-Oriented Strategy for the Construction of Spirocyclic 3(2H)-Furanones and 3-Pyrrolones. Cheminform. 38. DOI: 10.1002/CHIN.200729086 |
0.226 |
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2013 |
Harschneck T, Kirsch SF. Catalyst-Controlled 1,3-Polyol Syntheses Asymmetric Synthesis Ii: More Methods and Applications. 179-186. DOI: 10.1002/9783527652235.ch23 |
0.217 |
|
2008 |
Duschek A, Kirsch S. Verknüpfung der Konzepte: duale Katalyse mit carbophilen Lewis‐Säuren Angewandte Chemie. 120: 5787-5789. DOI: 10.1002/Ange.200801903 |
0.217 |
|
2006 |
Kirsch SF. IBX-Mediated α-Hydroxylation of α-Alkynyl Carbonyl Systems. A Convenient Method for the Synthesis of Tertiary Alcohols. Cheminform. 37. DOI: 10.1002/CHIN.200613052 |
0.209 |
|
2010 |
Haug TT, Kirsch SF. ChemInform Abstract: Synthesis and Chemistry of 3(2H)-Furanones Cheminform. 41: no-no. DOI: 10.1002/CHIN.201046247 |
0.209 |
|
2010 |
Lange A, Heydenreuter W, Menz H, Kirsch SF. ChemInform Abstract: Transition-Metal-Catalyzed Rearrangement of 1,1-(Oligomethylene)-4-aryl-2-butene-1,4-diols: Ring Expansion vs. Aryl Group Migration. Cheminform. 41. DOI: 10.1002/CHIN.201013063 |
0.206 |
|
2011 |
Kummerlöwe G, Crone B, Kretschmer M, Kirsch SF, Luy B. Rücktitelbild: Dipolare Restkopplungen als effektives Instrument der Konstitutionsanalyse: die unerwartete Bildung tricyclischer Verbindungen (Angew. Chem. 11/2011) Angewandte Chemie. 123: 2698-2698. DOI: 10.1002/Ange.201101025 |
0.204 |
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2011 |
Kummerlöwe G, Crone B, Kretschmer M, Kirsch SF, Luy B. Dipolare Restkopplungen als effektives Instrument der Konstitutionsanalyse: die unerwartete Bildung tricyclischer Verbindungen Angewandte Chemie. 123: 2693-2696. DOI: 10.1002/Ange.201007305 |
0.203 |
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2020 |
Wolf J, Huber F, Erochok N, Heinen F, Guérin V, Legault CY, Kirsch SF, Huber SM. Aktivierung einer Metall‐Halogen‐Bindung durch Halogenbrücken Angewandte Chemie. 132: 16638-16643. DOI: 10.1002/Ange.202005214 |
0.203 |
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2016 |
Bredenkamp A, Zhu Z, Kirsch SF. ChemInform Abstract: A Chiral Building Block for the Stereocontrolled Installation of the 1,3-Diol Motif. Cheminform. 47. DOI: 10.1002/CHIN.201622171 |
0.202 |
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2010 |
Crone B, Kirsch S, Umland K. Elektrophile Cyclisierung von 1,5-Eninen Angewandte Chemie. 122: 4765-4768. DOI: 10.1002/Ange.201001113 |
0.194 |
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2008 |
Kirsch S. Lange bekannt - aber erfolgreich: die Pinakolumlagerung Nachrichten Aus Der Chemie. 56: 1228-1231. DOI: 10.1002/Nadc.200860989 |
0.194 |
|
2006 |
Bach T, Kirsch S. Synthesis of Wailupemycins B Synfacts. 2006: 0412-0412. DOI: 10.1055/S-2006-934401 |
0.192 |
|
2004 |
Kirsch S, Bach T. Total Synthesis of (+)-Wailupemycin B (I). Cheminform. 35. DOI: 10.1002/CHIN.200405218 |
0.192 |
|
2004 |
Kirsch S, Ackermann O, Harms K, Bach T. Regioselective Isomerisation of Highly Substituted 1-Methylenecyclohexenepoxides to the Corresponding Allylic Alcohols. Influence of the Base and of the Protecting Groups Monatshefte F�R Chemie / Chemical Monthly. 135: 713-727. DOI: 10.1007/S00706-003-0153-7 |
0.187 |
|
2009 |
Duschek A, Kirsch SF. Novel oxygenations with IBX. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 10713-7. PMID 19760735 DOI: 10.1002/Chem.200901867 |
0.183 |
|
2000 |
Schneider G, Clément-Chomienne O, Hilfiger L, Schneider P, Kirsch S, Böhm H, Neidhart W. Evolutionäres De-novo-Design bioaktiver Moleküle: ein Ansatz zum virtuellen Screening Angewandte Chemie. 112: 4305-4309. DOI: 10.1002/1521-3757(20001117)112:22<4305::Aid-Ange4305>3.0.Co;2-N |
0.173 |
|
2011 |
Harschneck T, Kirsch SF. ChemInform Abstract: Elegant and Helpful: Biomimetic Synthetic Strategies Cheminform. 42: no-no. DOI: 10.1002/CHIN.201105229 |
0.166 |
|
2016 |
Erhardt H, Kirsch SF. ChemInform Abstract: Geminal Bis- and Tristriazoles: Long-Known but Still Uncommon Heterocyclic Entities Cheminform. 47. DOI: 10.1002/CHIN.201629278 |
0.157 |
|
2022 |
Kampschulte N, Berking T, Çelik IE, Kirsch SF, Schebb NH. Inhibition of cytochrome P450 monooxygenase-catalyzed oxylipin formation by flavonoids: Evaluation of structure-activity relationship towards CYP4F2-selective inhibitors. European Journal of Medicinal Chemistry. 238: 114332. PMID 35576701 DOI: 10.1016/j.ejmech.2022.114332 |
0.141 |
|
2020 |
Kutzner L, Goloshchapova K, Rund KM, Jübermann M, Blum M, Rothe M, Kirsch SF, Schunck WH, Kühn H, Schebb NH. Human lipoxygenase isoforms form complex patterns of double and triple oxygenated compounds from eicosapentaenoic acid. Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids. 158806. PMID 32841762 DOI: 10.1016/j.bbalip.2020.158806 |
0.128 |
|
2024 |
Bensberg K, Savvidis A, Ballaschk F, Gómez-Suárez A, Kirsch SF. Oxidation of Alcohols in Continuous Flow with a Solid Phase Hypervalent Iodine Catalyst. Chemistry (Weinheim An Der Bergstrasse, Germany). e202304011. PMID 38334293 DOI: 10.1002/chem.202304011 |
0.12 |
|
2023 |
Braun F, Jaschinski M, Täger P, Marmann V, Brandenstein MV, Köditz B, Fischer T, Muñoz-Vázquez S, Zimmermanns B, Dietlein M, Sudbrock F, Krapf P, Fischer D, Heidenreich A, Drzezga A, ... Kirsch S, et al. Synthesis and evaluation of radioiodinated estrogens for diagnosis and therapy of male urogenital tumours. Organic & Biomolecular Chemistry. PMID 36947011 DOI: 10.1039/d3ob00114h |
0.103 |
|
2010 |
Harschneck T, Kirsch SF. ChemInform Abstract: Success of Late C-H Oxidation. Cheminform. 41. DOI: 10.1002/chin.201015254 |
0.092 |
|
2007 |
Kirsch S, Bachert P. Diffraction-like phenomena in a periodic magnetization distribution at 1.5 T using the distant dipolar field (DDF) Journal of Magnetic Resonance. 185: 183-190. PMID 17110144 DOI: 10.1016/j.jmr.2006.10.011 |
0.079 |
|
2010 |
Harschneck T, Kirsch SF. ChemInform Abstract: Remarkably Chemoselective: Modification of Native Proteins Cheminform. 41: no-no. DOI: 10.1002/CHIN.201038245 |
0.077 |
|
2010 |
Harschneck T, Kirsch SF. ChemInform Abstract: Trifluoromethylation of Organic Molecules - What′s New? Cheminform. 41: no-no. DOI: 10.1002/CHIN.201047261 |
0.076 |
|
2014 |
Kirsch SF, Wegener M. Oxidation by Dehydrogenation Comprehensive Organic Synthesis: Second Edition. 7: 1-25. DOI: 10.1016/B978-0-08-097742-3.00701-1 |
0.07 |
|
2008 |
Kirsch S, Hull WE. Quantitative time- and frequency-domain analysis of the two-pulse COSY revamped by asymmetric Z -gradient echo detection NMR experiment: Theoretical and experimental aspects, time-zero data truncation artifacts, and radiation damping Journal of Chemical Physics. 129. PMID 18681658 DOI: 10.1063/1.2951993 |
0.066 |
|
2024 |
Hücker SM, Kirsch S. Single Cell Micro RNA Sequencing Library Preparation. Methods in Molecular Biology (Clifton, N.J.). 2752: 189-199. PMID 38194035 DOI: 10.1007/978-1-0716-3621-3_12 |
0.047 |
|
2015 |
Czyz ZT, Kirsch S, Polzer B. Principles of Whole-Genome Amplification. Methods in Molecular Biology (Clifton, N.J.). 1347: 1-14. PMID 26374306 DOI: 10.1007/978-1-4939-2990-0_1 |
0.041 |
|
2008 |
Münch C, Kirsch S, Fernandes AM, Schempp W. Evolutionary analysis of the highly dynamic CHEK2 duplicon in anthropoids. Bmc Evolutionary Biology. 8: 269. PMID 18831734 DOI: 10.1186/1471-2148-8-269 |
0.041 |
|
2002 |
Endris V, Wogatzky B, Leimer U, Bartsch D, Zatyka M, Latif F, Maher ER, Tariverdian G, Kirsch S, Karch D, Rappold GA. The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation. Proceedings of the National Academy of Sciences of the United States of America. 99: 11754-9. PMID 12195014 DOI: 10.1073/pnas.162241099 |
0.041 |
|
2009 |
Schmidt J, Kirsch S, Rappold GA, Schempp W. Complex evolution of a Y-chromosomal double homeobox 4 (DUX4)-related gene family in hominoids. Plos One. 4: e5288. PMID 19404400 DOI: 10.1371/journal.pone.0005288 |
0.04 |
|
2020 |
Werner-Klein M, Grujovic A, Irlbeck C, Obradović M, Hoffmann M, Koerkel-Qu H, Lu X, Treitschke S, Köstler C, Botteron C, Weidele K, Werno C, Polzer B, Kirsch S, Gužvić M, et al. Interleukin-6 trans-signaling is a candidate mechanism to drive progression of human DCCs during clinical latency. Nature Communications. 11: 4977. PMID 33020483 DOI: 10.1038/s41467-020-18701-4 |
0.031 |
|
2010 |
Kirsch S, Augath M, Seiffge D, Schilling L, Schad LR. In vivo chlorine-35, sodium-23 and proton magnetic resonance imaging of the rat brain. Nmr in Biomedicine. 23: 592-600. PMID 20232452 DOI: 10.1002/nbm.1500 |
0.029 |
|
2011 |
Kirsch S, Schad LR. Single-slice mapping of ultrashort T(2). Journal of Magnetic Resonance (San Diego, Calif. : 1997). 210: 133-6. PMID 21353799 DOI: 10.1016/j.jmr.2011.02.003 |
0.029 |
|
2021 |
Hücker SM, Fehlmann T, Werno C, Weidele K, Lüke F, Schlenska-Lange A, Klein CA, Keller A, Kirsch S. Single-cell microRNA sequencing method comparison and application to cell lines and circulating lung tumor cells. Nature Communications. 12: 4316. PMID 34262050 DOI: 10.1038/s41467-021-24611-w |
0.028 |
|
2015 |
Witte E, Kokolakis G, Witte K, Warszawska K, Friedrich M, Christou D, Kirsch S, Sterry W, Volk HD, Sabat R, Wolk K. Interleukin-29 induces epithelial production of CXCR3A ligands and T-cell infiltration. Journal of Molecular Medicine (Berlin, Germany). PMID 26612594 DOI: 10.1007/s00109-015-1367-y |
0.026 |
|
2011 |
Kirsch S, Hull WE. Erratum: "Quantitative time- and frequency-domain analysis of the two-pulse COSY revamped by asymmetic Z-gradient echo detection NMR experiment: theoretical and experimental aspects, time-zero data truncation artifacts, and radiation damping" [J. Chem. Phys. 129, 044505 (2008)]. The Journal of Chemical Physics. 133: 119902. PMID 20866160 DOI: 10.1063/1.3478222 |
0.023 |
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2013 |
Wolk K, Witte K, Witte E, Raftery M, Kokolakis G, Philipp S, Schönrich G, Warszawska K, Kirsch S, Prösch S, Sterry W, Volk HD, Sabat R. IL-29 is produced by T(H)17 cells and mediates the cutaneous antiviral competence in psoriasis. Science Translational Medicine. 5: 204ra129. PMID 24068736 DOI: 10.1126/scitranslmed.3006245 |
0.022 |
|
2002 |
Wimmer R, Kirsch S, Rappold GA, Schempp W. Direct evidence for the Homo-Pan clade. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 10: 55-61. PMID 11863072 DOI: 10.1023/a:1014222311431 |
0.021 |
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2016 |
Ebinger S, Özdemir EZ, Ziegenhain C, Tiedt S, Castro Alves C, Grunert M, Dworzak M, Lutz C, Turati VA, Enver T, Horny HP, Sotlar K, Parekh S, Spiekermann K, Hiddemann W, ... ... Kirsch S, et al. Characterization of Rare, Dormant, and Therapy-Resistant Cells in Acute Lymphoblastic Leukemia. Cancer Cell. 30: 849-862. PMID 27916615 DOI: 10.1016/J.Ccell.2016.11.002 |
0.02 |
|
2004 |
Kirsch S, Weiss B, Zumbach K, Rappold G. Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome Human Genetics. 114: 173-181. PMID 14579146 DOI: 10.1007/s00439-003-1028-z |
0.017 |
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2014 |
Baier S, Krämer P, Grudzenski S, Fatar M, Kirsch S, Schad LR. Chlorine and sodium chemical shift imaging during acute stroke in a rat model at 9.4 Tesla. Magma (New York, N.Y.). 27: 71-9. PMID 23934160 DOI: 10.1007/s10334-013-0398-z |
0.014 |
|
2005 |
Kirsch S, Weiss B, Miner TL, Waterston RH, Clark RA, Eichler EE, Münch C, Schempp W, Rappold G. Interchromosomal segmental duplications of the pericentromeric region on the human Y chromosome. Genome Research. 15: 195-204. PMID 15653831 DOI: 10.1101/gr.3302705 |
0.013 |
|
2008 |
Kirsch S, Pasantes J, Wolf A, Bogdanova N, Münch C, Markoff A, Pennekamp P, Krawczak M, Dworniczak B, Schempp W. Chromosomal evolution of the PKD1 gene family in primates. Bmc Evolutionary Biology. 8: 263. PMID 18822117 DOI: 10.1186/1471-2148-8-263 |
0.012 |
|
2008 |
Kirsch S, Münch C, Jiang Z, Cheng Z, Chen L, Batz C, Eichler EE, Schempp W. Evolutionary dynamics of segmental duplications from human Y-chromosomal euchromatin/heterochromatin transition regions. Genome Research. 18: 1030-42. PMID 18445620 DOI: 10.1101/Gr.076711.108 |
0.012 |
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2010 |
Sabat R, Grütz G, Warszawska K, Kirsch S, Witte E, Wolk K, Geginat J. Biology of interleukin-10 Cytokine and Growth Factor Reviews. 21: 331-344. PMID 21115385 DOI: 10.1016/j.cytogfr.2010.09.002 |
0.011 |
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2009 |
Augath M, Heiler P, Kirsch S, Schad LR. In vivo(39)K, (23)Na and (1)H MR imaging using a triple resonant RF coil setup. Journal of Magnetic Resonance (San Diego, Calif. : 1997). 200: 134-6. PMID 19501530 DOI: 10.1016/j.jmr.2009.05.005 |
0.011 |
|
2023 |
Porta C, Houshmand H, Povero M, Pradelli L, Monterosso F, Pinciroli M, Schuetze T, Kirsch S, Del Castillo JG. Benefits of MR-proADM-guided decision-making in the emergency department: clinical and economic evaluation in Italy, Germany, Spain, and the UK. Journal of Medical Economics. 26: 826-834. PMID 37314389 DOI: 10.1080/13696998.2023.2225354 |
0.01 |
|
2012 |
Kirsch S, Klein CA. Sequence error storms and the landscape of mutations in cancer. Proceedings of the National Academy of Sciences of the United States of America. 109: 14289-90. PMID 22912407 DOI: 10.1073/pnas.1212246109 |
0.01 |
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2007 |
Zechmann CM, Woenne EC, Brix G, Radzwill N, Ilg M, Bachert P, Peschke P, Kirsch S, Kauczor HU, Delorme S, Semmler W, Kiessling F. Impact of stroma on the growth, microcirculation, and metabolism of experimental prostate tumors. Neoplasia (New York, N.Y.). 9: 57-67. PMID 17325744 DOI: 10.1593/neo.06688 |
0.01 |
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2006 |
Kirsch S, Bachert P. Tissue contrast in MRI owing to intermolecular multiple-quantum coherences (iMQC) Zeitschrift Fur Medizinische Physik. 16: 188-198. PMID 16986458 |
0.01 |
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2002 |
Kirsch S, Weiss B, Schön K, Rappold GA. The definition of the Y chromosome growth-control gene (GCY) critical region: relevance of terminal and interstitial deletions. Journal of Pediatric Endocrinology & Metabolism : Jpem. 15: 1295-300. PMID 12510983 |
0.01 |
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