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Pyridiniumsalze als redoxaktive Reagenzien zur Übertragung funktioneller Gruppen.
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- Angewandte Chemie, 2020, v. 132, n. 24, p. 9350, doi. 10.1002/ange.201911660
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Palladiumkatalysierte C‐H‐Alkinylierung unaktivierter Alkene.
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- Angewandte Chemie, 2020, v. 132, n. 20, p. 7892, doi. 10.1002/ange.202000935
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Total Synthesis and Structural Revision of a Harziane Diterpenoid.
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- Angewandte Chemie, 2020, v. 132, n. 3, p. 1208, doi. 10.1002/ange.201912982
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Morpholine Ketene Aminal as Amide Enolate Surrogate in Iridium‐Catalyzed Asymmetric Allylic Alkylation.
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- Angewandte Chemie, 2019, v. 131, n. 28, p. 9637, doi. 10.1002/ange.201903090
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Total Synthesis of (−)‐Merochlorin A.
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- Angewandte Chemie, 2019, v. 131, n. 8, p. 2512, doi. 10.1002/ange.201813090
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- Article
Pyridyl Radical Cation for C−H Amination of Arenes.
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- Angewandte Chemie, 2019, v. 131, n. 2, p. 536, doi. 10.1002/ange.201810261
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Total Synthesis of Epicolactone.
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- Angewandte Chemie, 2018, v. 130, n. 40, p. 13343, doi. 10.1002/ange.201807709
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- Article
Trimethyl Orthoacetate and Ethylene Glycol Mono‐Vinyl Ether as Enolate Surrogates in Enantioselective Iridium‐Catalyzed Allylation.
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- Angewandte Chemie, 2018, v. 130, n. 26, p. 7780, doi. 10.1002/ange.201803558
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Total Synthesis of (+)‐Sarcophytin.
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- Angewandte Chemie, 2018, v. 130, n. 3, p. 831, doi. 10.1002/ange.201711372
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Stereoselective Synthesis of Piperidines by Iridium-Catalyzed Cyclocondensation.
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- Angewandte Chemie, 2017, v. 129, n. 38, p. 11673, doi. 10.1002/ange.201706374
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- Article
Total Synthesis of (+)-Dendrowardol C.
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- Angewandte Chemie, 2017, v. 129, n. 36, p. 11030, doi. 10.1002/ange.201705809
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Enantioselektive Chemo- und Biokatalyse: Partner in der Retrosynthese.
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- Angewandte Chemie, 2017, v. 129, n. 31, p. 9068, doi. 10.1002/ange.201612462
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Bioisosteric Exchange of C.
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- Angewandte Chemie, 2016, v. 128, n. 12, p. 4117, doi. 10.1002/ange.201511672
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Synthesis and Biological Evaluation of Bromo- and Fluorodanicalipin A.
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- Angewandte Chemie, 2016, v. 128, n. 7, p. 2601, doi. 10.1002/ange.201510608
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- Article
Formation of α-SF<sub>5</sub>-Enolate Enables Preparation of 3-SF<sub>5</sub>-Quinolin-2-ones, 3-SF<sub>5</sub>-Quinolines, and 3-SF<sub>5</sub>-Pyridin-2-ones: Evaluation of their Physicochemical Properties.
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- Angewandte Chemie, 2016, v. 128, n. 6, p. 2153, doi. 10.1002/ange.201510380
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Biological Investigations of (+)-Danicalipin A Enabled Through Synthesis.
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- Angewandte Chemie, 2016, v. 128, n. 2, p. 649, doi. 10.1002/ange.201509082
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Stereodivergent Dual Catalytic α-Allylation of Protected α-Amino- and α-Hydroxyacetaldehydes.
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- Angewandte Chemie, 2015, v. 127, n. 48, p. 14571, doi. 10.1002/ange.201506933
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Pentafulvene for the Synthesis of Complex Natural Products: Total Syntheses of (±)-Pallambins A and B.
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- Angewandte Chemie, 2015, v. 127, n. 38, p. 11379, doi. 10.1002/ange.201505126
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Iridium-Catalyzed Enantioselective Allylic Alkylation with Functionalized Organozinc Bromides.
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- Angewandte Chemie, 2015, v. 127, n. 26, p. 7754, doi. 10.1002/ange.201501851
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- Article
Total Synthesis of (±)-Hippolachnin A.
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- Angewandte Chemie, 2015, v. 127, n. 8, p. 2408, doi. 10.1002/ange.201410419
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Stereodivergent Total Synthesis of Δ<sup>9</sup>-Tetrahydrocannabinols.
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- Angewandte Chemie, 2014, v. 126, n. 50, p. 14118, doi. 10.1002/ange.201408380
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Recent Advances in the Total Synthesis of Chlorosulfolipids (Eur. J. Org. Chem. 9/2012).
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- European Journal of Organic Chemistry, 2012, v. 2012, n. 9, p. n/a, doi. 10.1002/ejoc.201290018
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Recent Advances in the Total Synthesis of Chlorosulfolipids.
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- European Journal of Organic Chemistry, 2012, v. 2012, n. 9, p. 1685, doi. 10.1002/ejoc.201101525
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- Article
Construction of Spiro[pyrrolidine-3,3'-oxindoles] - Recent Applications to the Synthesis of Oxindole Alkaloids.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 12, p. 2209, doi. 10.1002/ejoc.200300050
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Cover Picture: Construction of Spiro[pyrrolidine-3,3'-oxindoles] - Recent Applications to the Synthesis of Oxindole Alkaloids (Eur. J. Org. Chem. 12/2003).
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 12, p. 2183, doi. 10.1002/ejoc.200390226
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Total Synthesis and Stereochemical Revision of the Chlorinated Sesquiterpene (±)-Gomerone C.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 52, p. 13066, doi. 10.1002/anie.201207203
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- Article
Enantioselective Allylic Thioetherification: The Effect of Phosphoric Acid Diester on Iridium-Catalyzed Enantioconvergent Transformations.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 34, p. 8652, doi. 10.1002/anie.201202092
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- Article
Arynes and Cyclohexyne in Natural Product Synthesis.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 16, p. 3766, doi. 10.1002/anie.201107485
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Direct, Enantioselective Iridium-Catalyzed Allylic Amination of Racemic Allylic Alcohols.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 14, p. 3470, doi. 10.1002/anie.201108287
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Total Synthesis and Stereochemical Reassignment of (±)-Indoxamycin B.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 14, p. 3474, doi. 10.1002/anie.201109175
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Total Synthesis of (−)-Dendrobine.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 14, p. 3436, doi. 10.1002/anie.201108564
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Total Synthesis of (+)-Daphmanidin E.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 48, p. 11501, doi. 10.1002/anie.201104681
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Cobalt-Catalyzed Coupling of Alkyl Iodides with Alkenes: Deprotonation of Hydridocobalt Enables Turnover.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 47, p. 11125, doi. 10.1002/anie.201105235
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Catalytic Asymmetric Intramolecular Hydroacylation with Rhodium/Phosphoramidite-Alkene Ligand Complexes.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 45, p. 10670, doi. 10.1002/anie.201104595
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Synthesis of Trifluoroethyl-Substituted Ketones from Aldehydes and Cyclohexanones.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 39, p. 9085, doi. 10.1002/anie.201103526
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Iridium Diamine Catalyst for the Asymmetric Transfer Hydrogenation of Ketones.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 38, p. 8979, doi. 10.1002/anie.201102732
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- Article
Synthesis of Undecachlorosulfolipid A: Re-evaluation of the Nominal Structure.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 34, p. 7940, doi. 10.1002/anie.201102521
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- Article
Enantioselective Allylic Etherification: Selective Coupling of Two Unactivated Alcohols.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 24, p. 5568, doi. 10.1002/anie.201007716
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- Article
Cascade Formation of Isoxazoles: Facile Base-Mediated Rearrangement of Substituted Oxetanes.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 23, p. 5379, doi. 10.1002/anie.201100260
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- Article
Asymmetric Autocatalysis Enables an Improved Synthesis of Efavirenz.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 13, p. 2957, doi. 10.1002/anie.201006689
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- Article
Total Syntheses of Guanacastepenes N and O.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 13, p. 2962, doi. 10.1002/anie.201007644
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- Article
Enantioselective Cobalt-Catalyzed Preparation of Trifluoromethyl-Substituted Cyclopropanes.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 5, p. 1101, doi. 10.1002/anie.201004269
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Probing the Biology of Natural Products: Molecular Editing by Diverted Total Synthesis.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 50, p. 9592, doi. 10.1002/anie.200904761
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Oxetanes as Versatile Elements in Drug Discovery and Synthesis.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 48, p. 9052, doi. 10.1002/anie.200907155
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Total Synthesis of Nominal Banyaside B: Structural Revision of the Glycosylation Site.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 48, p. 9229, doi. 10.1002/anie.201004047
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Rhodium-Catalyzed Cyclopropenation of Alkynes: Synthesis of Trifluoromethyl-Substituted Cyclopropenes.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 25, p. 4294, doi. 10.1002/anie.201000787
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Cyclohexyne Cycloinsertion by an Annulative Ring Expansion Cascade.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 24, p. 4092, doi. 10.1002/anie.201001137
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Synthesis of Azaspirocycles and their Evaluation in Drug Discovery.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 20, p. 3524, doi. 10.1002/anie.200907108
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Iron-Catalyzed Cyclopropanation with Trifluoroethylamine Hydrochloride and Olefins in Aqueous Media: In Situ Generation of Trifluoromethyl Diazomethane.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 5, p. 938, doi. 10.1002/anie.200905573
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Nucleophilic Opening of Oxabicyclic Ring Systems.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 34, p. 6296, doi. 10.1002/anie.200902046
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