Supporting Information
Experimental details and detailed spectroscopic data of all compounds are available as Supporting Information. Single crystal data for 1h and 2b (CCDC 1516680 and 1516681) has been deposited in the Cambridge Crystallographic Data Center.
| Supporting Information File 1: Experimental details and detailed spectroscopic data of all compounds. | ||
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| Supporting Information File 2: Single crystal data for 1h and 2b. | ||
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Cite the Following Article
Unpredictable cycloisomerization of 1,11-dien-6-ynes by a common cobalt catalyst
Abdusalom A. Suleymanov, Dmitry V. Vasilyev, Valentin V. Novikov, Yulia V. Nelyubina and Dmitry S. Perekalin
Beilstein J. Org. Chem. 2017, 13, 639–643.
https://doi.org/10.3762/bjoc.13.62
How to Cite
Suleymanov, A. A.; Vasilyev, D. V.; Novikov, V. V.; Nelyubina, Y. V.; Perekalin, D. S. Beilstein J. Org. Chem. 2017, 13, 639–643. doi:10.3762/bjoc.13.62
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- Matsuda, T.; Yonekubo, N. Ruthenium-catalysed cyclisation reactions of 1,11-dien-6-ynes leading to biindenes. Organic & biomolecular chemistry 2020, 18, 1760–1764. doi:10.1039/d0ob00179a
- Chang, C.-A.; Gürtzgen, S.; Johnson, E. P.; Vollhardt, K. P. C. Stoichiometric and Catalytic (η5-Cyclopentadienyl)cobalt-Mediated Cycloisomerizations of Ene-Yne-Ene Type Allyl Propargyl Ethers. Synthesis 2019, 52, 399–416. doi:10.1055/s-0039-1690727
- Ai, W.; Zhong, R.; Liu, X.; Liu, Q. Hydride Transfer Reactions Catalyzed by Cobalt Complexes. Chemical reviews 2018, 119, 2876–2953. doi:10.1021/acs.chemrev.8b00404
