Ambient gold-catalyzed O-vinylation of cyclic 1,3-diketone: A vinyl ether synthesis

Scholarly Works

• Stein, P. M.; Pascher, J.; Stracke, J.; Levacher, V. S.; Wagner, J. A.; Rominger, F.; Oeser, T.; Rudolph, M.; Hashmi, A. S. K. Gold Catalysis: 2,3‐ or 1,4‐Addition to Butadiynes. Advanced Synthesis & Catalysis 2022, 364, 3817–3839. doi:10.1002/adsc.202200497
• Ahrens, A.; Schwarz, J.; Lustosa, D. M.; Pourkaveh, R.; Hoffmann, M.; Rominger, F.; Rudolph, M.; Dreuw, A.; Hashmi, A. S. K. Synthesis of Fulvene Vinyl Ethers by Gold Catalysis. Chemistry (Weinheim an der Bergstrasse, Germany) 2020, 26, 5280–5287. doi:10.1002/chem.202000338
• Dong, B.; Xi, Y.; Su, Y.; Akhmedov, N. G.; Petersen, J. L.; Shi, X. Gold/gallium-catalyzed annulation of 1,3-dicarbonyl compounds and cyclopropylacetylenes for synthesis of substituted cyclopentenes. RSC Advances 2016, 6, 17386–17389. doi:10.1039/c6ra00896h
• Hosseyni, S.; Ding, S.; Su, Y.; Akhmedov, N. G.; Shi, X. Triazole–gold promoted intermolecular propargyl alcohol addition to alkyne: the reaction cascade toward substituted allenes. Chemical communications (Cambridge, England) 2015, 52, 296–299. doi:10.1039/c5cc08233a
• Xi, Y.; Su, Y.; Yu, Z.; Dong, B.; McClain, E. J.; Lan, Y.; Shi, X. Chemoselective Carbophilic Addition of α-Diazoesters through Ligand-Controlled Gold Catalysis†. Angewandte Chemie (International ed. in English) 2014, 53, 9817–9821. doi:10.1002/anie.201404946
• Xi, Y.; Su, Y.; Yu, Z.; Dong, B.; McClain, E. J.; Lan, Y.; Shi, X. Chemoselective Carbophilic Addition of α‐Diazoesters through Ligand‐Controlled Gold Catalysis. Angewandte Chemie 2014, 126, 9975–9979. doi:10.1002/ange.201404946
• Cai, R.; Wang, D.; Chen, Y.; Yan, W.; Geise, N. R.; Sharma, S.; Li, H.; Petersen, J. L.; Li, M.; Shi, X. Facile synthesis of fluorescent active triazapentalenes through gold-catalyzed triazole-alkyne cyclization. Chemical communications (Cambridge, England) 2014, 50, 7303–7305. doi:10.1039/c4cc03175j
• Genin, E.; Michelet, V. Patai's Chemistry of Functional Groups - Gold-Catalyzed Addition of HX to Alkynes. Patai's Chemistry of Functional Groups 2014, 1–60. doi:10.1002/9780470682531.pat0814
• Xi, Y.; Dong, B.; McClain, E. J.; Wang, Q.; Gregg, T. L.; Akhmedov, N. G.; Petersen, J. L.; Shi, X. Gold‐Catalyzed Intermolecular CS Bond Formation: Efficient Synthesis of α‐Substituted Vinyl Sulfones. Angewandte Chemie 2014, 126, 4745–4749. doi:10.1002/ange.201310142
• Su, Y.; Zhang, Y.; Akhmedov, N. G.; Petersen, J. L.; Shi, X. Ambient intermolecular [2 + 2] cycloaddition: an example of carbophilicity and oxophilicity competition in Au/Ag catalysis. Organic letters 2014, 16, 2478–2481. doi:10.1021/ol500854m
• Xi, Y.; Dong, B.; McClain, E. J.; Wang, Q.; Gregg, T. L.; Akhmedov, N. G.; Petersen, J. L.; Shi, X. Gold-Catalyzed Intermolecular CS Bond Formation: Efficient Synthesis of α-Substituted Vinyl Sulfones. Angewandte Chemie (International ed. in English) 2014, 53, 4657–4661. doi:10.1002/anie.201310142
• Fang, W.; Presset, M.; Guérinot, A.; Bour, C.; Bezzenine-Lafollée, S.; Gandon, V. Silver‐Free Two‐Component Approach in Gold Catalysis: Activation of [LAuCl] Complexes with Derivatives of Copper, Zinc, Indium, Bismuth, and Other Lewis Acids. Chemistry (Weinheim an der Bergstrasse, Germany) 2014, 20, 5439–5446. doi:10.1002/chem.201304831

Explore citations to this article at