Supporting Information
Supporting Information File 1: Detailed experimental procedures. | ||
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Supporting Information File 2: NMR spectral data for substrates 6a–s. | ||
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Supporting Information File 3: NMR spectral data for products 7a–s. | ||
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Cite the Following Article
Gold(I)-catalyzed formation of furans by a Claisen-type rearrangement of ynenyl allyl ethers
Florin M. Istrate and Fabien Gagosz
Beilstein J. Org. Chem. 2011, 7, 878–885.
https://doi.org/10.3762/bjoc.7.100
How to Cite
Istrate, F. M.; Gagosz, F. Beilstein J. Org. Chem. 2011, 7, 878–885. doi:10.3762/bjoc.7.100
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- Zhai, T.; Ge, C.; Qian, P.; Zhou, B.; Ye, L. Brønsted Acid-Catalyzed Intramolecular Hydroalkoxylation/Claisen Rearrangement of Ynamides★. Acta Chimica Sinica 2023, 81, 1101. doi:10.6023/a23040188
- Dyachenko, V. D.; Baryshev, B. N.; Nenajdenko, V. G. [3,3]-Sigmatropic rearrangements: a variety of methods and recent advances. Russian Chemical Reviews 2022, 91, RCR5039. doi:10.1070/rcr5039
- Yu, B.; Mohamed, S.; Ardisson, J.; Lannou, M.-I.; Sorin, G. Silver oxide(I) promoted Conia-ene/radical cyclization for a straightforward access to furan derivatives. Chemical communications (Cambridge, England) 2022, 58, 1374–1377. doi:10.1039/d1cc06379k
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- Zhong, Z.; Peng, X.-S. Comprehensive Heterocyclic Chemistry IV - Furans and Their Benzo Derivatives: Synthesis. Comprehensive Heterocyclic Chemistry IV; Elsevier, 2022; pp 307–411. doi:10.1016/b978-0-12-409547-2.14769-9
- Pandit, Y. B.; Liu, R.-S. Dynamic Kinetic Resolution in Gold-Catalyzed (4 + 2)-Annulations between Alkynyl Benzaldehydes and Allenamides to Yield Enantioenriched All-Carbon Diarylalkylmethane Derivatives. Organic letters 2021, 24, 548–553. doi:10.1021/acs.orglett.1c03963
- Shi, C.-Y.; Li, L.; Kang, W.; Zheng, Y.-X.; Ye, L.-W. Claisen rearrangement triggered by transition metal-catalyzed alkyne alkoxylation. Coordination Chemistry Reviews 2021, 446, 214131. doi:10.1016/j.ccr.2021.214131
- Milcendeau, P.; Gandon, V.; Guinchard, X. Gold‐Catalyzed Carboamination of Allenes by Tertiary Amines Proceeding with Benzylic Group Migration. Advanced Synthesis & Catalysis 2021, 363, 2893–2902. doi:10.1002/adsc.202100007
- Hrizi, A.; Thiery, E.; Romdhani-Younes, M.; Jacquemin, J.; Thibonnet, J. Efficient Synthesis of Polysubstituted Furans through a Base-Promoted Oxacyclization of (Z)-2-En-4-yn-1-ols. European Journal of Organic Chemistry 2021, 2021, 3798–3806. doi:10.1002/ejoc.202100471
- Hu, C.; Farshadfar, K.; Dietl, M. C.; Cervantes-Reyes, A.; Wang, T.; Adak, T.; Rudolph, M.; Rominger, F.; Li, J.; Ariafard, A.; Hashmi, A. S. K. Gold-Catalyzed [5,5]-Rearrangement. ACS Catalysis 2021, 11, 6510–6518. doi:10.1021/acscatal.1c01108
- Qi, L.-J.; Shi, C.-Y.; Chen, P.-F.; Li, L.; Fang, G.; Qian, P.-C.; Deng, C.; Zhou, J.-M.; Ye, L.-W. Gold-Catalyzed 1,1-Carboalkoxylation of Oxetane-Ynamides via Exocyclic Metal Carbenes: Divergent and Atom-Economical Synthesis of Tricyclic N-Heterocycles. ACS Catalysis 2021, 11, 3679–3686. doi:10.1021/acscatal.1c00461
- Kim, H.; Jang, J.; Shin, S. Gold-Catalyzed Asymmetric Thioallylation of Propiolates via Charge-Induced Thio-Claisen Rearrangement. Journal of the American Chemical Society 2020, 142, 20788–20795. doi:10.1021/jacs.0c09783
- Praveen, C. Regio‐ and Site‐selective Molecular Rearrangements by Homogeneous Gold Catalysis. Asian Journal of Organic Chemistry 2020, 9, 1953–1998. doi:10.1002/ajoc.202000444
- Cornils, B. doi:10.1002/9783527809080.cataz07240
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