Year |
Citation |
Score |
2025 |
Özkaya Y, Ballaschk F, Wagner C, Kotthaus AF, Gómez-Suárez A, Kirsch SF. Lewis-Base-Catalyzed Asymmetric Allylation of Isatins with Allyltrichlorosilane. Organic Letters. PMID 40074547 DOI: 10.1021/acs.orglett.5c00338 |
0.373 |
|
2024 |
Kunz KA, Springer BL, Klahn P, Aldemir H, Mohr F, Kirsch SF. Synthesis of -Substituted 1,2,3-Triazoles. Organic Letters. PMID 39378272 DOI: 10.1021/acs.orglett.4c03204 |
0.724 |
|
2024 |
Tapera M, Borghi F, Mayer-Figge JL, Mittendorf F, Celik IE, Gómez-Suárez A, Kirsch SF. A Formal Synthesis of (+)-Hannokinol Using a Chiral Horner-Wittig Reagent. Molecules (Basel, Switzerland). 29. PMID 39125113 DOI: 10.3390/molecules29153710 |
0.316 |
|
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 |
0.3 |
|
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 |
0.384 |
|
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 |
0.409 |
|
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 |
0.347 |
|
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 |
0.361 |
|
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 |
0.438 |
|
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 |
0.393 |
|
2019 |
Ottenbruch M, Mohr F, Kirsch SF. Synthesis of Sulfonylisoureas via Sulfo-Click Reactions Synthesis. 52: 695-702. DOI: 10.1055/S-0039-1691505 |
0.448 |
|
2019 |
Ballaschk F, Kirsch SF. Oxidation of secondary alcohols using solid-supported hypervalent iodine catalysts Green Chemistry. 21: 5896-5903. DOI: 10.1039/C9Gc02605C |
0.327 |
|
2019 |
Biallas P, Heider J, Kirsch SF. Functional polyamides withgem-diazido units: synthesis and diversification Polymer Chemistry. 10: 60-64. DOI: 10.1039/C8Py01087K |
0.321 |
|
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 |
0.416 |
|
2018 |
Holzschneider K, Mohr F, Kirsch SF. Synthesis and Reactivity of 3,3-Diazidooxindoles. Organic Letters. PMID 30365325 DOI: 10.1021/Acs.Orglett.8B03013 |
0.45 |
|
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 |
0.435 |
|
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 |
0.358 |
|
2017 |
Wagner C, Kotthaus AF, Kirsch SF. The asymmetric reduction of imidazolinones with trichlorosilane. Chemical Communications (Cambridge, England). PMID 28387397 DOI: 10.1039/C7Cc01561E |
0.469 |
|
2017 |
Biallas P, Häring AP, Kirsch SF. Cleavage of 1,3-dicarbonyls through oxidative amidation. Organic & Biomolecular Chemistry. PMID 28362452 DOI: 10.1039/C7Ob00731K |
0.408 |
|
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 |
0.446 |
|
2017 |
Ballaschk F, Erhardt H, Kirsch SF. Synthesis of substituted pyrazines from N-allyl malonamides Rsc Advances. 7: 55594-55597. DOI: 10.1039/C7Ra11529F |
0.434 |
|
2017 |
Biallas P, Kirsch SF. Hydrogenolysis of geminal diazides Tetrahedron Letters. 58: 4209-4211. DOI: 10.1016/J.Tetlet.2017.09.066 |
0.409 |
|
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 |
0.399 |
|
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 |
0.481 |
|
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 |
0.387 |
|
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 |
0.438 |
|
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 |
0.34 |
|
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 |
0.304 |
|
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 |
0.434 |
|
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 |
0.317 |
|
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 |
0.438 |
|
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 |
0.372 |
|
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 |
0.47 |
|
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 |
0.364 |
|
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 |
0.345 |
|
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 |
0.37 |
|
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 |
0.396 |
|
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 |
0.707 |
|
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 |
0.386 |
|
2015 |
Klahn P, Kirsch SF. ChemInform Abstract: IBX-Mediated Dehydrogenation of Substituted β-Oxonitriles. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201506179 |
0.654 |
|
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 |
0.736 |
|
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 |
0.395 |
|
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 |
0.729 |
|
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 |
0.485 |
|
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 |
0.718 |
|
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 |
0.654 |
|
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 |
0.312 |
|
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 |
0.414 |
|
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 |
0.441 |
|
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 |
0.347 |
|
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 |
0.371 |
|
2012 |
Klahn P, Duschek A, Liébert C, Kirsch SF. Total synthesis of (+)-cyperolone. Organic Letters. 14: 1250-3. PMID 22324453 DOI: 10.1021/Ol300058T |
0.73 |
|
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 |
0.72 |
|
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 |
0.387 |
|
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 |
0.41 |
|
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 |
0.496 |
|
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 |
0.314 |
|
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 |
0.686 |
|
2011 |
Harschneck T, Kirsch SF, Wegener M. Electrophilic Cyclization of 1,6-Enynes Synlett. 2011: 1151-1153. DOI: 10.1055/S-0030-1259938 |
0.379 |
|
2011 |
Harschneck T, Kirsch SF, Wegener M. ChemInform Abstract: Electrophilic Cyclization of 1,6-Enynes. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201138032 |
0.308 |
|
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 |
0.735 |
|
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 |
0.652 |
|
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 |
0.74 |
|
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 |
0.753 |
|
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 |
0.355 |
|
2010 |
Haug TT, Kirsch SF. Total synthesis of (+)-chloriolide Organic and Biomolecular Chemistry. 8: 991-993. PMID 20165786 DOI: 10.1039/B925644J |
0.395 |
|
2010 |
Menz H, Kirsch SF. Synthesis of Polyrhacitides A and B Synfacts. 2010: 504-504. DOI: 10.1055/S-0029-1219710 |
0.326 |
|
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 |
0.341 |
|
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 |
0.364 |
|
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 |
0.353 |
|
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 |
0.749 |
|
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 |
0.477 |
|
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 |
0.343 |
|
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 |
0.707 |
|
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 |
0.437 |
|
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 |
0.404 |
|
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 |
0.487 |
|
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 |
0.347 |
|
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 |
0.353 |
|
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 |
0.41 |
|
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 |
0.444 |
|
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 |
0.422 |
|
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 |
0.72 |
|
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 |
0.437 |
|
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 |
0.33 |
|
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 |
0.492 |
|
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 |
0.73 |
|
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 |
0.448 |
|
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 |
0.424 |
|
2006 |
Kirsch SF. Syntheses of polysubstituted furans: Recent developments Organic and Biomolecular Chemistry. 4: 2076-2080. PMID 16729118 DOI: 10.1039/B602596J |
0.367 |
|
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 |
0.49 |
|
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 |
0.321 |
|
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 |
0.381 |
|
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 |
0.321 |
|
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 |
0.589 |
|
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 |
0.523 |
|
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 |
0.566 |
|
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 |
0.591 |
|
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 |
0.576 |
|
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 |
0.533 |
|
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 |
0.408 |
|
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 |
0.584 |
|
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