Supporting Information
Supporting Information File 1: Spectral data. | ||
Format: PDF | Size: 1.2 MB | Download |
Cite the Following Article
Asymmetric Au-catalyzed cycloisomerization of 1,6-enynes: An entry to bicyclo[4.1.0]heptene
Alexandre Pradal, Chung-Meng Chao, Patrick Y. Toullec and Véronique Michelet
Beilstein J. Org. Chem. 2011, 7, 1021–1029.
https://doi.org/10.3762/bjoc.7.116
How to Cite
Pradal, A.; Chao, C.-M.; Toullec, P. Y.; Michelet, V. Beilstein J. Org. Chem. 2011, 7, 1021–1029. doi:10.3762/bjoc.7.116
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Liang, R.-X.; Ding, C.; Cai, H.-J.; Wang, J.-Y.; Li, Q.-C.; Yu, G.-Y.; Jia, Y.-X. Pd-Catalyzed Enantioselective Desymmetrizing 1,7-Enyne Cycloisomerization of Alkyne-Tethered Cyclopentenes. Organic letters 2024, 26, 4400–4405. doi:10.1021/acs.orglett.4c01507
- Taniguchi, N.; Ueda, M.; Michigami, K.; Mori, S.; Ohashi, M. Asymmetric cyclization catalyzed by a chiral phosphoric acid–gold(I) hybrid complex as a multifunctional catalyst. Bulletin of the Chemical Society of Japan 2024, 97. doi:10.1093/bulcsj/uoae026
- Jin, D.; Cao, S.; Cheng, F.; Xue, Z.; Li, R.; Pu, Y.; Zhu, D.; Bao, W.; Xu, X.; Wang, S. A Gold(I)‐Catalyzed Cyclization/Semipinacol Rearrangement Cascade of 1,6‐Enynes to Access Spiro[4.5]decanes and 7‐Azaspiro[4.5]decanes. Advanced Synthesis & Catalysis 2023, 365, 312–317. doi:10.1002/adsc.202201266
- Ji, H.; Knutson, P. C.; Harrington, C. M.; Ke, Y.-T.; Ferreira, E. M. The Analysis of Two Distinct Strategies toward the Enantioselective Formal Total Synthesis of (+)-Gelsenicine. Tetrahedron 2023, 134, 133278. doi:10.1016/j.tet.2023.133278
- Galéa, R.; Blond, G. Gold(I)‐Catalyzed Domino Reaction: An Access to Furooxepines. Advanced Synthesis & Catalysis 2022, 364, 1532–1536. doi:10.1002/adsc.202200019
- Yu, J.; Czekelius, C. Insights into the Gold‐Catalyzed Cycloisomerization of 3‐Allyl‐1,4‐diynes for the Synthesis of Bicyclic Hydrocarbons. European Journal of Organic Chemistry 2022, 2022. doi:10.1002/ejoc.202200027
- Pallova, L.; Abella, L.; Jean, M.; Vanthuyne, N.; Barthes, C.; Vendier, L.; Autschbach, J.; Crassous, J.; Bastin, S.; César, V. Helical Chiral N-Heterocyclic Carbene Ligands in Enantioselective Gold Catalysis. Chemistry (Weinheim an der Bergstrasse, Germany) 2022, 28, e202200166. doi:10.1002/chem.202200166
- Michelet, V. Gold-Catalyzed Reactions Towards Diversity: From Simple Substrates to Functionalized Carbo- and Heterocycles. Chemical record (New York, N.Y.) 2021, 21, 3884–3896. doi:10.1002/tcr.202100253
- Dupeux, A.; Michelet, V. Gold-Catalyzed Domino Cycloisomerization/Alkoxylation: An Entry to 3,4-Dihydro-1H-[1,4]oxazino[4,3-a]indole. The Journal of organic chemistry 2021, 86, 17738–17747. doi:10.1021/acs.joc.1c02030
- Mato, M.; Franchino, A.; García-Morales, C.; Echavarren, A. M. Gold-Catalyzed Synthesis of Small Rings. Chemical reviews 2020, 121, 8613–8684. doi:10.1021/acs.chemrev.0c00697
- Wu, R.; Chen, K.; Ma, J.; Yu, Z.-X.; Zhu, S. Synergy of activating substrate and introducing C–H···O interaction to achieve Rh 2 (II)-catalyzed asymmetric cycloisomerization of 1, n -enynes. Science China Chemistry 2020, 63, 1230–1239. doi:10.1007/s11426-020-9794-3
- Zhou, F.; Zhu, L.; Pan, B.-W.; Shi, Y.; Liu, Y.-L.; Zhou, J. Catalytic enantioselective construction of vicinal quaternary carbon stereocenters. Chemical science 2020, 11, 9341–9365. doi:10.1039/d0sc03249b
- Laher, R.; Marin, C.; Michelet, V. When Gold Meets Perfumes: Synthesis of Olfactive Compounds via Gold-Catalyzed Cycloisomerization Reactions. Organic letters 2020, 22, 4058–4062. doi:10.1021/acs.orglett.0c00843
- Liu, R.; Yang, D.; Chang, F.; Giordano, L.; Liu, G.; Tenaglia, A. An Electrophilic Ruthenium Complex that Enables the Cycloisomerization of 1,6-Enynes to Access Azabicyclo[4.1.0]heptenes. Asian Journal of Organic Chemistry 2019, 8, 2011–2016. doi:10.1002/ajoc.201900529
- Li, C.-L.; Yu, Z.-X. Asymmetric Synthesis of Azepine-Fused Cyclobutanes from Yne-Methylenecyclopropanes Involving Cyclopropanation/C–C Cleavage/Wagner–Meerwein Rearrangement and Reaction Mechanism. The Journal of organic chemistry 2019, 84, 9913–9928. doi:10.1021/acs.joc.9b01071
- Lee, Y.-C.; Knauer, L.; Louven, K.; Golz, C.; Strohmann, C.; Waldmann, H.; Kumar, K. Gold(I)-Catalyzed and Nucleophile-Guided Ligand-Directed Divergent Synthesis. European Journal of Organic Chemistry 2018, 2018, 5688–5699. doi:10.1002/ejoc.201801080
- Toullec, P. Y.; Michelet, V. Gold‐Catalyzed Polycyclization Toward Natural Products Synthesis. Israel Journal of Chemistry 2018, 58, 578–585. doi:10.1002/ijch.201800002
- Pellissier, H.; Lattanzi, A.; Dalpozzo, R. doi:10.1002/9783527802029.ch1
- Zhuang, Z.; Li, C.-L.; Xiang, Y.; Wang, Y.-H.; Yu, Z.-X. An enyne cycloisomerization/[5+1] reaction sequence to synthesize tetrahydroisoquinolinones from enyne-enes and CO. Chemical communications (Cambridge, England) 2017, 53, 2158–2161. doi:10.1039/c6cc09925d
- Hines, J. M.; Eason, J. J.; Siebert, M. R. One Lump or Two? A Plurality of Pathways in Gold(III)-Catalyzed Cyclization Transforming Propargyl Acetates to a Carene-like Bicyclo[4.1.0]heptane. Organometallics 2017, 36, 920–926. doi:10.1021/acs.organomet.6b00946