![Tandem Ring‐Opening–Ring‐Closing Metathesis for Functional Metathesis Catalysts - Nagarkar - 2016 - Angewandte Chemie International Edition - Wiley Online Library Tandem Ring‐Opening–Ring‐Closing Metathesis for Functional Metathesis Catalysts - Nagarkar - 2016 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/6936c1b8-b5fd-48ff-b7db-a7f1b18d599e/anie201604112-toc-0001-m.png)
Tandem Ring‐Opening–Ring‐Closing Metathesis for Functional Metathesis Catalysts - Nagarkar - 2016 - Angewandte Chemie International Edition - Wiley Online Library
![Syntheses of polycyclic carbocycles via domino ring-closing metathesis. | Download Scientific Diagram Syntheses of polycyclic carbocycles via domino ring-closing metathesis. | Download Scientific Diagram](https://www.researchgate.net/publication/346253951/figure/fig2/AS:983885546532865@1611588002417/Syntheses-of-polycyclic-carbocycles-via-domino-ring-closing-metathesis.png)
Syntheses of polycyclic carbocycles via domino ring-closing metathesis. | Download Scientific Diagram
Ring-Closing Metathesis of Allylsilanes/Electrophilic Desilylation To Prepare exo-Methylidenecycloalkanes. Short Syntheses of Teucladiol and Poitediol | Journal of the American Chemical Society
Control of Olefin Geometry in Macrocyclic Ring-Closing Metathesis Using a Removable Silyl Group | Journal of the American Chemical Society
![Selective ring-rearrangement or ring-closing metathesis of bicyclo[3.2.1]octenes - Chemical Communications (RSC Publishing) DOI:10.1039/D0CC04624H Selective ring-rearrangement or ring-closing metathesis of bicyclo[3.2.1]octenes - Chemical Communications (RSC Publishing) DOI:10.1039/D0CC04624H](https://pubs.rsc.org/image/article/2020/CC/d0cc04624h/d0cc04624h-s2_hi-res.gif)