| Year |
Citation |
Score |
| 2021 |
Klychnikov MK, Pohl R, Císařová I, Jahn U. α,γ-Dioxygenated amides via tandem Brook rearrangement/radical oxygenation reactions and their application to syntheses of γ-lactams. Beilstein Journal of Organic Chemistry. 17: 688-704. PMID 33777244 DOI: 10.3762/bjoc.17.58 |
0.353 |
|
| 2020 |
Šimek M, Bártová K, Pohl R, Císařová I, Jahn U. Tandem Anionic oxy-Cope Rearrangement/Oxygenation Reactions as a Versatile Method for Approaching Diverse Scaffolds. Angewandte Chemie (International Ed. in English). 59: 6160-6165. PMID 31994304 DOI: 10.1002/anie.201916188 |
0.314 |
|
| 2020 |
Klychnikov MK, Pohl R, Cisarova I, Jahn U. Application of the Brook Rearrangement in Tandem with Single Electron Transfer Oxidative and Radical Processes European Journal of Organic Chemistry. 2020: 2854-2866. DOI: 10.1002/Ejoc.202000126 |
0.334 |
|
| 2019 |
Dokli I, Pohl R, Klepetářová B, Jahn U. First total synthesis of ent-asperparaline C and assignment of the absolute configuration of asperparaline C. Chemical Communications (Cambridge, England). 55: 3931-3934. PMID 30874266 DOI: 10.1039/c9cc00945k |
0.324 |
|
| 2018 |
Amatov T, Jangra H, Pohl R, Cisařová I, Zipse H, Jahn U. Unique Stereoselective Homolytic C-O Bond Activation in Diketopiperazine-Derived Alkoxyamines by Adjacent Amide Pyramidalization. Chemistry: a European Journal. 24: 15336-15345. PMID 30092124 DOI: 10.1002/Chem.201803284 |
0.714 |
|
| 2018 |
Jagtap PR, Císařová I, Jahn U. Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps. Organic & Biomolecular Chemistry. 16: 750-755. PMID 29308468 DOI: 10.1039/c7ob02848b |
0.33 |
|
| 2018 |
Hidasová D, Janák M, Jahn E, Císařová I, Jones PG, Jahn U. Diastereoselective Radical Couplings Enable the Asymmetric Synthesis of anti‐β‐Amino‐α‐hydroxy Carboxylic Acid Derivatives European Journal of Organic Chemistry. 2018: 5222-5230. DOI: 10.1002/Ejoc.201801139 |
0.414 |
|
| 2017 |
Smrček J, Pohl R, Jahn U. Total syntheses of all tri-oxygenated 16-phytoprostane classes via a common precursor constructed by oxidative cyclization and alkyl-alkyl coupling reactions as the key steps. Organic & Biomolecular Chemistry. 15: 9408-9414. PMID 29095476 DOI: 10.1039/c7ob02505j |
0.339 |
|
| 2017 |
Amatov T, Pohl R, Cisařová I, Jahn U. Sequential Oxidative and Reductive Radical Cyclization Approach toward Asperparaline C and Synthesis of Its 8-Oxo Analogue. Organic Letters. 19: 1152-1155. PMID 28207265 DOI: 10.1021/acs.orglett.7b00187 |
0.73 |
|
| 2016 |
Amatov T, Gebauer M, Pohl R, Cisařová I, Jahn U. Oxidative radical cyclizations of diketopiperazines bearing an amidomalonate unit. Heterointermediate reaction sequences toward the asperparalines and stephacidins. Free Radical Research. 50: S6-S17. PMID 27806645 DOI: 10.1080/10715762.2016.1223295 |
0.73 |
|
| 2016 |
Řehová L, Dračínský M, Jahn U. A general approach to iridoids by applying a new Julia olefination and a tandem anion-radical-carbocation crossover reaction. Organic & Biomolecular Chemistry. 14: 9612-9621. PMID 27714288 DOI: 10.1039/C6Ob01599A |
0.482 |
|
| 2015 |
Amatov T, Pohl R, Císařová I, Jahn U. Synthesis of bridged diketopiperazines by using the persistent radical effect and a formal synthesis of bicyclomycin. Angewandte Chemie. 54: 12153-12157. PMID 26418182 DOI: 10.1002/Anie.201504883 |
0.726 |
|
| 2015 |
Buček A, Matoušková P, Vogel H, Šebesta P, Jahn U, Weißflog J, Svatoš A, Pichová I. Evolution of moth sex pheromone composition by a single amino acid substitution in a fatty acid desaturase. Proceedings of the National Academy of Sciences of the United States of America. PMID 26417103 DOI: 10.1073/Pnas.1514566112 |
0.315 |
|
| 2015 |
Holan M, Pohl R, Císa?ová I, Klepetá?ová B, Jones PG, Jahn U. Highly Functionalized Cyclopentane Derivatives by Tandem Michael Addition/Radical Cyclization/Oxygenation Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 9877-88. PMID 26012714 DOI: 10.1002/Chem.201500424 |
0.442 |
|
| 2015 |
Jahn E, Smrček J, Pohl R, Císařová I, Jones PG, Jahn U. Facile and Highly Diastereoselective Synthesis of syn- and cis-1,2-Diol Derivatives from Protected α-Hydroxy Ketones European Journal of Organic Chemistry. 2015: 7785-7798. DOI: 10.1002/Ejoc.201501174 |
0.368 |
|
| 2015 |
Mahamulkar SG, Císařová I, Jahn U. The Lithiation Reactivity and Selectivity of Differentially Branched Alkyldiphenylphosphine Oxides – A Simple and Versatile Approach to ortho-Functionalized Arylphosphine Oxides Advanced Synthesis & Catalysis. 357: 793-799. DOI: 10.1002/Adsc.201400861 |
0.345 |
|
| 2014 |
Kafka F, Holan M, Hidasová D, Pohl R, Císařová I, Klepetářová B, Jahn U. Oxidative catalysis using the stoichiometric oxidant as a reagent: an efficient strategy for single-electron-transfer-induced tandem anion-radical reactions. Angewandte Chemie (International Ed. in English). 53: 9944-8. PMID 25070407 DOI: 10.1002/Anie.201403776 |
0.41 |
|
| 2014 |
Jagtap PR, Ford L, Deister E, Pohl R, Císa?ová I, Hodek J, Weber J, Mackman R, Bahador G, Jahn U. Highly functionalized and potent antiviral cyclopentane derivatives formed by a tandem process consisting of organometallic, transition-metal-catalyzed, and radical reaction steps. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 10298-304. PMID 25043655 DOI: 10.1002/Chem.201402595 |
0.428 |
|
| 2014 |
Trujillo C, Sánchez‐Sanz G, Karpavičienė I, Jahn U, Čikotienė I, Rulíšek L. Divergent Pathways and Competitive Mechanisms of Metathesis Reactions between 3‐Arylprop‐2‐ynyl Esters and Aldehydes: An Experimental and Theoretical Study Chemistry: a European Journal. 20: 10360-10370. PMID 25043400 DOI: 10.1002/Chem.201402551 |
0.351 |
|
| 2014 |
Amatov T, Jahn U. Gliotoxin: nature's way of making the epidithio bridge. Angewandte Chemie (International Ed. in English). 53: 3312-4. PMID 24615992 DOI: 10.1002/anie.201310982 |
0.677 |
|
| 2014 |
Vazdar K, Kunetskiy R, Saame J, Kaupmees K, Leito I, Jahn U. Very strong organosuperbases formed by combining imidazole and guanidine bases: synthesis, structure, and basicity. Angewandte Chemie. 53: 1435-1438. PMID 24339377 DOI: 10.1002/Anie.201307212 |
0.337 |
|
| 2014 |
Řehová L, Jahn U. Elucidation of the Reaction Mechanism of ortho→α Transmetalation Reactions of Alkyl Aryl Sulfone Carbanions European Journal of Organic Chemistry. 2014: 4610-4623. DOI: 10.1002/Ejoc.201402171 |
0.378 |
|
| 2014 |
Řehová L, Císařová I, Jahn U. Divergent Reactivity of Alkyl Aryl Sulfones with Bases: Selective Functionalization of ortho-Aryl and α-Alkyl Units Enabled by a Unique Carbanion Transmetalation European Journal of Organic Chemistry. 2014: 1461-1476. DOI: 10.1002/Ejoc.201301553 |
0.358 |
|
| 2013 |
Lagoutte R, Šebesta P, Jiroš P, Kalinová B, Jirošová A, Straka J, Černá K, Šobotník J, Cvačka J, Jahn U. Total synthesis, proof of absolute configuration, and biosynthetic origin of stylopsal, the first isolated sex pheromone of strepsiptera. Chemistry: a European Journal. 19: 8515-8524. PMID 23630024 DOI: 10.1002/Chem.201204196 |
0.689 |
|
| 2012 |
Cvačka J, Jiroš P, Kalinová B, Straka J, Černá K, Šebesta P, Tomčala A, Vašíčková S, Jahn U, Šobotník J. Stylopsal: the first identified female-produced sex pheromone of strepsiptera. Journal of Chemical Ecology. 38: 1483-1491. PMID 23143664 DOI: 10.1007/S10886-012-0214-7 |
0.328 |
|
| 2012 |
Khobragade DA, Mahamulkar SG, Pospíšil L, Císařová I, Rulíšek L, Jahn U. Acceptor-substituted ferrocenium salts as strong, single-electron oxidants: synthesis, electrochemistry, theoretical investigations, and initial synthetic application. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 12267-77. PMID 22899019 DOI: 10.1002/Chem.201201499 |
0.411 |
|
| 2012 |
Jahn U, Rudakov D, Jones PG. Oxidative tandem alkoxide conjugate addition to nitroalkenes/radical 5-exo cyclizations—a versatile synthesis of functionalized 3-nitrotetrahydrofurans Tetrahedron. 68: 1521-1539. DOI: 10.1016/J.TET.2011.12.010 |
0.324 |
|
| 2012 |
Jahn U, Rudakov D, Jones PG. 4-(1-Haloalkyl)-3-nitrotetrahydrofurans as versatile scaffolds for the synthesis of diversely functionalized tetrahydrofurans Tetrahedron. 68: 447-463. DOI: 10.1016/J.Tet.2011.11.023 |
0.456 |
|
| 2012 |
Holan M, Pohl R, Císařová I, Jahn U. Polyfunctional β‐Dicarbonyl Compounds by Michael Addition Reactions of Ester Enolates to α‐Benzylidene and α‐Alkylidene‐β‐dicarbonyl Compounds European Journal of Organic Chemistry. 2012: 3459-3475. DOI: 10.1002/EJOC.201403454 |
0.374 |
|
| 2012 |
Dinca E, Hartmann P, Smrček J, Dix I, Jones PG, Jahn U. General and Efficient α-Oxygenation of Carbonyl Compounds by TEMPO Induced by Single-Electron-Transfer Oxidation of Their Enolates (Eur. J. Org. Chem. 24/2012) European Journal of Organic Chemistry. 2012. DOI: 10.1002/Ejoc.201290063 |
0.327 |
|
| 2012 |
Dinca E, Hartmann P, Smrček J, Dix I, Jones PG, Jahn U. General and Efficient α‐Oxygenation of Carbonyl Compounds by TEMPO Induced by Single‐Electron‐Transfer Oxidation of Their Enolates European Journal of Organic Chemistry. 2012: 4461-4482. DOI: 10.1002/Ejoc.201200736 |
0.436 |
|
| 2012 |
Jahn U, Rudakov D, Jones PG. ChemInform Abstract: Oxidative Tandem Alkoxide Conjugate Addition to Nitroalkenes/Radical 5-exo Cyclizations - A Versatile Synthesis of Functionalized 3-Nitrotetrahydrofurans. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201227098 |
0.347 |
|
| 2011 |
Jahn U. Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? – A Fruitful Interplay Anyway Topics in Current Chemistry. 320: 121-189. PMID 22025066 DOI: 10.1007/128_2011_261 |
0.362 |
|
| 2011 |
Amatov T, Jahn U. Perhaloalkylation of metal enolates-unconventional and versatile. Angewandte Chemie (International Ed. in English). 50: 4542-4. PMID 21520362 DOI: 10.1002/anie.201007672 |
0.669 |
|
| 2010 |
Jahn U, Dinca E. Toward the elucidation of the metabolism of 15-E(2)-isoprostane: the total synthesis of the methyl ester of a potential central metabolite. The Journal of Organic Chemistry. 75: 4480-91. PMID 20527974 DOI: 10.1021/Jo1006569 |
0.364 |
|
| 2010 |
Puget B, Jahn U. β,β-DisilylatedSulfones as Versatile Building Blocks in Organic Chemistry - ANew Sulfonyl Carbanion Transmetalation Synlett. 2010: 2579-2582. DOI: 10.1055/S-0030-1258772 |
0.318 |
|
| 2010 |
Zöllner MJ, Frähmcke JS, Elstner M, Jahn U, Jones PG, Becker E, Kowalsky W, Johannes H. A New Synthetic Approach to Thiophene‐Nickel(II)porphyrin Hybrid Molecules and their Electrochemical and Computational Investigation Macromolecular Chemistry and Physics. 211: 359-371. DOI: 10.1002/Macp.200900480 |
0.325 |
|
| 2010 |
Zöllner MJ, Becker E, Jahn U, Kowalsky W, Johannes H. New Versatile Strategy towards Zinc(II)-, Copper(II)- and Cobalt(II)-Metallated Thiophene/Porphyrin-Hybrids European Journal of Organic Chemistry. 2010: 4426-4435. DOI: 10.1002/Ejoc.200901237 |
0.361 |
|
| 2010 |
Jahn U. ChemInform Abstract: Tandem Anionic Michael Addition/Radical Cyclizations: A New and Efficient Strategy for the Synthesis of Functionalized Cyclopentanes. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200152061 |
0.307 |
|
| 2010 |
JAHN U, CURRAN DP. ChemInform Abstract: Towards a Tandem-Radical Macrocyclization-Transannular Cyclization Approach to Steroids: Transannular Cyclizations of a Macrocyclic Core. Cheminform. 27: no-no. DOI: 10.1002/chin.199613100 |
0.303 |
|
| 2009 |
Zöllner MJ, Jahn U, Becker E, Kowalsky W, Johannes H. Simplified methods for the functionalisation of 3-hexoxythiophenes at the 5-position and further reactions to alkynyl and vinyl derivatives Chemical Communications. 565-7. PMID 19283292 DOI: 10.1039/B817089D |
0.333 |
|
| 2009 |
Jahn U, Dinca E. Total synthesis of 15-F2t-isoprostane by using a new oxidative cyclization of distonic radical anions as the key step. Chemistry: a European Journal. 15: 58-62. PMID 19072797 DOI: 10.1002/Chem.200802139 |
0.454 |
|
| 2009 |
Jahn U, Kafka F, Pohl R, Jones PG. N,3,4-Trisubstituted pyrrolidines by electron transfer-induced oxidative cyclizations of N-allylic β-amino ester enolates Tetrahedron. 65: 10917-10929. DOI: 10.1016/J.Tet.2009.10.034 |
0.404 |
|
| 2004 |
Jahn U, Hartmann P, Kaasalainen E. Efficient oxidative radical cyclizations of ester enolates with carbocation desilylation as termination: synthesis of cyclopentanoid monoterpenes and analogues. Organic Letters. 6: 257-60. PMID 14723542 DOI: 10.1021/ol036233n |
0.378 |
|
| 2002 |
Jahn U. Tandem anionic Michael addition/radical cyclizations: a new and efficient strategy for the synthesis of functionalized cyclopentanes. Chemical Communications (Cambridge, England). 1600-1. PMID 12240401 DOI: 10.1039/B104415J |
0.345 |
|
| 2002 |
Jahn U, Hartmann P, Dix I, Jones P. Oxidative Enolate Cyclizations of 6,8-Nonadienoates: Towards the Synthesis of Prostanes European Journal of Organic Chemistry. 2002: 718-735. DOI: 10.1002/1099-0690(200202)2002:4<718::AID-EJOC718>3.0.CO;2-6 |
0.303 |
|
| 2000 |
Jahn U, Müller M, Aussieker S. The Combination of Anionic and Radical Reactions to Oxidative Tandem Processes Exemplified by the Synthesis of Functionalized Pyrrolidines Journal of the American Chemical Society. 122: 5212-5213. DOI: 10.1021/JA000565V |
0.329 |
|
| 2000 |
Jahn U, Mueller M, Aussieker S. ChemInform Abstract: The Combination of Anionic and Radical Reactions to Oxidative Tandem Processes Exemplified by the Synthesis of Functionalized Pyrrolidines. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200037120 |
0.335 |
|
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