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Cavicularin (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Cavicularin" in English language version.

refsWebsite
Global rank English rank
6doi.org
2nd place
2nd place
4nih.gov
4th place
4th place
3harvard.edu
18th place
17th place

doi.org (Global: 2nd place; English: 2nd place)

  • M. Toyota; T. Yoshida; Y. Kan; S. Takaoka; Y. Asakawa (1996). "(+)-Cavicularin: A Novel Optically Active Cyclic Bibenzyl-Dihydrophenanthrene Derivative from the Liverwort Cavicularia densa Steph". Tetrahedron Letters. 37 (27): 4745–4748. doi:10.1016/0040-4039(96)00956-2.[dead link]
  • David C. Harrowven; Timothy Woodcock; Peter D. Howes (2005). "Total Synthesis of Cavicularin and Riccardin C: Addressing the Synthesis of an Arene That Adopts a Boat Configuration". Angewandte Chemie. 44 (25): 3899–3901. Bibcode:2005ACIE...44.3899H. doi:10.1002/anie.200500466. PMID 15900530.
  • Kostiuk, S. L.; Woodcock, T.; Dudin, L. F.; Howes, P. D.; Harrowven, D. C. (2011). "Unified Syntheses of Cavicularin and Riccardin C: Addressing the Synthesis of an Arene Adopting a Boat Configuration". Chemistry: A European Journal. 17 (39): 10906–10915. Bibcode:2011ChEuJ..1710906K. doi:10.1002/chem.201101550. PMID 21932232.
  • Takiguchi, H.; Ohmori, K.; Suzuki, K. (2013). "Synthesis and Determination of the Absolute Configuration of Cavicularin by a Symmetrization/Asymmetrization Approach". Angew. Chem. Int. Ed. 52 (40): 10472–10476. Bibcode:2013ACIE...5210472T. doi:10.1002/anie.201304929. PMID 23956143.
  • Zhao, Peng; Beaudry, Christopher M. (2013). "Total Synthesis of (±)-Cavicularin: Control of Pyrone Diels–Alder Regiochemistry Using Isomeric Vinyl Sulfones". Organic Letters. 15 (2): 402–405. doi:10.1021/ol303390a. PMID 23301524.
  • Harada, Kenichi; Makino, Kosho; Shima, Naoki; Okuyama, Haruka; Esumi, Tomoyuki; Kubo, Miwa; Hioki, Hideaki; Asakawa, Yoshinori; Fukuyama, Yoshiyasu (2013). "Total synthesis of riccardin C and (±)-cavicularin via Pd-catalyzed Ar–Ar cross couplings". Tetrahedron. 69 (34): 6959–6968. doi:10.1016/j.tet.2013.06.064.

harvard.edu (Global: 18th place; English: 17th place)

ui.adsabs.harvard.edu

nih.gov (Global: 4th place; English: 4th place)

pubmed.ncbi.nlm.nih.gov

  • David C. Harrowven; Timothy Woodcock; Peter D. Howes (2005). "Total Synthesis of Cavicularin and Riccardin C: Addressing the Synthesis of an Arene That Adopts a Boat Configuration". Angewandte Chemie. 44 (25): 3899–3901. Bibcode:2005ACIE...44.3899H. doi:10.1002/anie.200500466. PMID 15900530.
  • Kostiuk, S. L.; Woodcock, T.; Dudin, L. F.; Howes, P. D.; Harrowven, D. C. (2011). "Unified Syntheses of Cavicularin and Riccardin C: Addressing the Synthesis of an Arene Adopting a Boat Configuration". Chemistry: A European Journal. 17 (39): 10906–10915. Bibcode:2011ChEuJ..1710906K. doi:10.1002/chem.201101550. PMID 21932232.
  • Takiguchi, H.; Ohmori, K.; Suzuki, K. (2013). "Synthesis and Determination of the Absolute Configuration of Cavicularin by a Symmetrization/Asymmetrization Approach". Angew. Chem. Int. Ed. 52 (40): 10472–10476. Bibcode:2013ACIE...5210472T. doi:10.1002/anie.201304929. PMID 23956143.
  • Zhao, Peng; Beaudry, Christopher M. (2013). "Total Synthesis of (±)-Cavicularin: Control of Pyrone Diels–Alder Regiochemistry Using Isomeric Vinyl Sulfones". Organic Letters. 15 (2): 402–405. doi:10.1021/ol303390a. PMID 23301524.