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3 results for “ring-closing metathesis”
E/Z Switchable Ring-closing Metathesis in 1,1′-Bis(but-3-enyl)ferrocenes: Synthesis and Characterization of Axially Chiral ansa[6]-Ferrocenes. Raw Diffraction Data.
<p>Diffraction data for article <em>E</em>/<em>Z</em> Switchable Ring-Closing Metathesis in 1,1′-Bis(but-3-enyl)ferrocenes: Synthesis and Characterization of Axially Chiral <em>ansa</em>[6]-Ferrocenes doi: <a href="https://doi.org/10.1021/acs.organomet.2c00163">10.1021/acs.organomet.2c00163</a>. The crystal structures have been deposited in CSD with CCDC numbers 2093772-2093775, 2094024-2094027 and 2119739.</p>
Synthesis of N-Substituted Indoles via Aqueous Ring-Closing Metathesis
<p>Data underlying the figures in the publication “Synthesis of N-Substituted Indoles via Aqueous Ring-Closing Metathesis?”, published in <em>Catal. Lett.,</em> <strong>2021, </strong>151, 1–7.</p> <p> <a href="https://doi.org/10.1007/s10562-020-03271-3">https://doi.org/10.1007/s10562-020-03271-3</a></p> <p>Table of contents:</p> <p><strong>1. Dataset 1</strong>; Word file containing the synthetic protocols, catalysis studies and characterization of the compounds.</p> <p> </p> <p> </p>
Schrock molybdenum alkylidene catalyst enables selective formation of macrocyclic unsaturated lactones by ring-closing metathesis at high-concentration
<p>Data supporting findings described in Green Chemistry, 2023, 25, 2299-2304. <a title="Link to landing page via DOI" href="https://doi.org/10.1039/D2GC02988J">https://doi.org/10.1039/D2GC02988J</a></p> <p>The research was performed within OPUS project and was funded by National Science Centre, Poland, grant number DEC-2019/33/B/ST4/00874.</p>
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