Ring-opening metathesis of some strained bicyclic systems; stereocontrolled access to diolefinated saturated heterocycles with multiple stereogenic centers

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• Kiss, L.; Benke, Z.; Nonn, M.; Remete, A. M.; Fustero, S. Diversity-Oriented Synthesis of Highly Functionalized Alicycles across Dipolar Cycloaddition/Metathesis Reaction. Synlett 2021, 32, 1911–1933. doi:10.1055/s-0040-1706041
• Kiss, L.; Benke, Z.; Remete, A. M.; Fülöp, F. Diversity-oriented Functionalization of Cyclodienes Through Selective Cycloaddition/Ring-opening/Cross-metathesis Protocols; Transformation of a "Flatland" into Three-dimensional Scaffolds With Stereo- and Regiocontrol. Chemical record (New York, N.Y.) 2020, 20, 1129–1141. doi:10.1002/tcr.202000070
• Dragutan, V.; Dragutan, I.; Demonceau, A.; Delaude, L. Combining enyne metathesis with long-established organic transformations: a powerful strategy for the sustainable synthesis of bioactive molecules. Beilstein journal of organic chemistry 2020, 16, 738–755. doi:10.3762/bjoc.16.68
• Herndon, J. W. The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2018. Coordination Chemistry Reviews 2019, 401, 213051. doi:10.1016/j.ccr.2019.213051
• Benke, Z.; Nonn, M.; Fülöp, F.; Kiss, L. An Insight into Selective Olefin Bond Functionalization of Cyclodienes through Nitrile Oxide 1,3‐Dipolar Cycloadditions. ChemistrySelect 2019, 4, 2886–2891. doi:10.1002/slct.201900688

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