Relay cross metathesis reactions of vinylphosphonates

Raj K. Malla, Jeremy N. Ridenour and Christopher D. Spilling
Beilstein J. Org. Chem. 2014, 10, 1933–1941. https://doi.org/10.3762/bjoc.10.201

Supporting Information

Supporting Information File 1: Experimental procedures, characterization data, 1H and 13C spectra for all new compounds.
Format: PDF Size: 3.2 MB Download

Cite the Following Article

Relay cross metathesis reactions of vinylphosphonates
Raj K. Malla, Jeremy N. Ridenour and Christopher D. Spilling
Beilstein J. Org. Chem. 2014, 10, 1933–1941. https://doi.org/10.3762/bjoc.10.201

How to Cite

Malla, R. K.; Ridenour, J. N.; Spilling, C. D. Beilstein J. Org. Chem. 2014, 10, 1933–1941. doi:10.3762/bjoc.10.201

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

  • Grela, K.; Kajetanowicz, A.; Szadkowska, A.; Czaban-Jóźwiak, J. Organic Reactions - Alkene Cross-Metathesis Reactions. Organic Reactions 2021, 1–1189. doi:10.1002/0471264180.or106.01
  • Bahou, K. A.; Braddock, D. C.; Meyer, A. G.; Savage, G. P.; Shi, Z.; He, T. A Relay Strategy Actuates Pre-Existing Trisubstituted Olefins in Monoterpenoids for Cross-Metathesis with Trisubstituted Alkenes. The Journal of organic chemistry 2020, 85, 4906–4917. doi:10.1021/acs.joc.0c00067
  • Chattopadhyay, S. K.; Ghosh, S.; Sil, S. Cross metathesis-mediated synthesis of hydroxamic acid derivatives. Beilstein journal of organic chemistry 2018, 14, 3070–3075. doi:10.3762/bjoc.14.285
  • Adler, P.; Fadel, A.; Prunet, J.; Rabasso, N. From acyclic to cyclic α-amino vinylphosphonates by using ring-closing metathesis. Organic & biomolecular chemistry 2017, 15, 387–395. doi:10.1039/c6ob02548j
  • Chrobak, E.; Bębenek, E.; Kadela-Tomanek, M.; Latocha, M.; Jelsch, C.; Wenger, E.; Boryczka, S. Betulin Phosphonates; Synthesis, Structure, and Cytotoxic Activity. Molecules (Basel, Switzerland) 2016, 21, 1123. doi:10.3390/molecules21091123
  • Herndon, J. W. The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2014. Coordination Chemistry Reviews 2016, 317, 1–121. doi:10.1016/j.ccr.2015.09.012
  • Mulla, K.; Aleshire, K. L.; Forster, P. M.; Kang, J. Y. Utility of Bifunctional N-Heterocyclic Phosphine (NHP)-Thioureas for Metal-Free Carbon-Phosphorus Bond Construction toward Regio- and Stereoselective Formation of Vinylphosphonates. The Journal of organic chemistry 2015, 81, 77–88. doi:10.1021/acs.joc.5b02184
  • Anitha, M.; Kotikalapudi, R.; Swamy, K. C. K. FeCl 3 catalysed regioselective allylation of phenolic substrates with ( α -hydroxy)allylphosphonates. Journal of Chemical Sciences 2015, 127, 1465–1475. doi:10.1007/s12039-015-0903-1

Patents

  • CONG CHANGJIE; GUO CHUNTAI; GAO XIULING; DONG JING; CHEN XIANGLAN. ELECTROLYTE ADDITIVE, USE THEREOF AND NON-AQUEOUS ELECTROLYTE CONTAINING ADDITIVE. EP 4040560 A4, Oct 25, 2023.
Other Beilstein-Institut Open Science Activities