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Ferrocene derivatives of liquid chiral molecules allow assignment of absolute configuration by X-ray crystallography
Tetrahedron: Asymmetry 2017, 28 (10), 1321-1329, DOI: 10.1016/j.tetasy.2017.09.002. -
Ruthenium-Catalyzed Peri- and Ortho-Alkynylation with Bromoalkynes via Insertion and Elimination
GO TO OPEN ACCESS Org. Lett. 2017, 19 (20), 5561-5564, DOI: 10.1021/acs.orglett.7b02655. -
Gold(I)-Catalyzed Synthesis of Indenes and Cyclopentadienes: Access to (±)-Laurokamurene B and the Skeletons of Cycloaurenones and Dysiherbols
GO TO OPEN ACCESS Angew. Chem. Int. Ed. 2017, 56 (46), 14591-14595 , DOI: 10.1002/anie.201708947. -
Enantioselective Synthesis of Cyclobutenes by Intermolecular [2+2] Cycloaddition with Non-C2 Symmetric Digold Catalysts
GO TO OPEN ACCESS J. Am. Chem. Soc. 2017, 139, 13628-13631, DOI: 10.1021/jacs.7b07651. -
Nonacene generated by on-surface dehydrogenation
ACS Nano 2017, 11 (9), 9321-9329, DOI: 10.1021/acsnano.7b04728.* Highlighted in Chemistry Views.
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Cyclobutene vs. 1,3-Diene Formation in the Gold-Catalyzed Reaction of Alkynes with Alkenes: The Complete Mechanistic Picture
GO TO OPEN ACCESS J. Am. Chem. Soc. 2017, 139 (30), 10302-10311, DOI: 10.1021/jacs.7b03005. -
Stereoselective cis-Vinylcyclopropanation via a Gold(I)-Catalyzed Retro-Buchner Reaction under Mild Conditions
GO TO OPEN ACCESS ACS Catal. 2017, 7, 3668-3675, DOI: 10.1021/acscatal.7b00737. -
Broad Scope Gold(I)-Catalysed Polyenyne Cyclisations for the Formation of up to Four Carbon-Carbon Bonds
GO TO OPEN ACCESS Org. Biomol. Chem. 2017, 15, 2163-2167, DOI: 10.1039/C7OB00235A. -
Strategies for the Synthesis of Higher Acenes
COVER GO TO OPEN ACCESS Eur. J. Org. Chem. 2017, 14-24, DOI: 10.1002/ejoc.201601129.* Highlighted in EurJOC Readers‘ Choice 2019
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Functional-Group-Tolerant, Silver-Catalyzed N-N Bond Formation by Nitrene Transfer to Amines
GO TO OPEN ACCESS J. Am. Chem. Soc. 2017, 139, 2216-2223, DOI: 10.1021/jacs.6b08219. -
Gold(I) Carbenoids: On-Demand Access to Gold(I) Carbenes in Solution
GO TO OPEN ACCESS Angew. Chem., Intl. Ed. 2017, DOI: 10.1002/ange.201611705.