Dendralene (English Wikipedia)

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

refsWebsite
Global rank English rank
2nd place
2nd place
4th place
4th place
5th place
5th place
942nd place
597th place
102nd place
76th place

anu.edu.au (Global: 942nd place; English: 597th place)

openresearch-repository.anu.edu.au

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

  • Hopf, H.; Sherburn, M. S. (2012). "Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular Complexity". Angewandte Chemie International Edition in English. 51 (10): 2298–2338. doi:10.1002/anie.201102987. PMID 22337341.
  • Preparation and Synthetic Value of π-Bond-Rich Branched Hydrocarbons Michael S. Sherburn Accounts of Chemical Research 2015 48 (7), 1961-1970 doi:10.1021/acs.accounts.5b00242
  • Bailey, William J.; Economy, James (1955). "Pyrolysis of Esters. III. Synthesis of 2-Vinylbutadiene". J. Am. Chem. Soc. 77 (5): 1133–1136. doi:10.1021/ja01610a014.
  • Blomquist, A. T.; Verdol, Joseph A. (1955). "2-Vinyl-1,3-butadiene". J. Am. Chem. Soc. 77 (1): 81–83. doi:10.1021/ja01606a025.
  • Bailey, William J.; Economy, James; Hermes, Mathew E. (1962). "Polymers. IV. Polymeric Diels-Alder Reactions". J. Org. Chem. 27 (9): 3295–3299. doi:10.1021/jo01056a074.
  • Mieko Arisawa, Takumichi Sugihara and Masahiko Yamaguchi Synthesis of cross-conjugated trienes by dimerization of allenes with palladium-phenol catalyst Chem. Commun. 1998; 2615-2616 doi:10.1039/A807527A
  • Rekha Singh and Sunil K. Ghosh Synthesis of substituted [3]dendralenes and their unique cycloaddition reactions Chem. Commun. 2011; Advance Article doi:10.1039/C1CC14211A
  • Bradford, Tanya A.; Payne, Alan D.; Willis, Anthony C.; Paddon-Row, Michael N.; Sherburn, Michael S. (2007). "Cross-Coupling for Cross-Conjugation:? Practical Synthesis and Diels?Alder Reactions of [3]Dendralenes". Organic Letters. 9 (23): 4861–4864. doi:10.1021/ol7021998. PMID 17929828.
  • Kassem Beydoun, Hui-Jun Zhang, Basker Sundararaju, Bernard Demerseman, Mathieu Achard, Zhenfeng Xi and Christian Bruneau Efficient ruthenium-catalyzed synthesis of [3]dendralenes from 1,3-dienic allylic carbonates Chem. Commun. 2009; 6580-6582 doi:10.1039/B913595B
  • Payne, Alan D.; Willis, Anthony C.; Sherburn, Michael S. (2005). "Practical Synthesis and Diels−Alder Chemistry of [4]Dendralene". Journal of the American Chemical Society. 127 (35): 12188–12189. doi:10.1021/ja053772+. ISSN 0002-7863. PMID 16131173.
  • Molecular Structure of 3,4-Dimethylenehexa-1,5-diene ([4]Dendralene), C8H10, in the Gas Phase As Determined by Electron Diffraction and ab Initio Calculations Paul T. Brain,Bruce A. Smart,Heather E. Robertson,Martin J. Davis,†, David W. H. Rankin,*, William J. Henry, and Ian Gosney The Journal of Organic Chemistry 1997 62 (9), 2767-2773 doi:10.1021/jo962091h
  • Practical Synthesis of the Dendralene Family Reveals Alternation in Behavior Alan D. Payne, Gomotsang Bojase, Michael N. Paddon-Row, and Michael S. Sherburn Angew. Chem. Int. Ed. 2009, 48, doi:10.1002/anie.200901733
  • Discovery and Computational Rationalization of Diminishing Alternation in [n]Dendralenes Mehmet F. Saglam, Thomas Fallon, Michael N. Paddon-Row, and Michael S. Sherburn Journal of the American Chemical Society 2016 138 (3), 1022-1032 doi:10.1021/jacs.5b11889
  • Brummond, Kay M.; You, Lingfeng (2005). "Consecutive Rh(I)-catalyzed Alder-ene/Diels–Alder/Diels–Alder reaction sequence affording rapid entry to polycyclic compounds". Tetrahedron. 61 (26): 6180–6185. doi:10.1016/j.tet.2005.03.141.
  • Hopf, H.; Yildizhan, Ş. (2011). "Highly Functionalized, Angularly Anellated Aromatic Compounds from Dendralenes". European Journal of Organic Chemistry. 2011 (11): 2029–2034. doi:10.1002/ejoc.201001536.
  • A novel and facile stereocontrolled synthetic method for polyhydro-quinolines and pyridopyridazines via a diene-transmissive Diels–Alder reaction involving inverse electron-demand hetero Diels–Alder cycloaddition of cross-conjugated azatrienes Tetrahedron, Volume 64, Issue 41, 6 October 2008, Pages 9705-9716 Satoru Kobayashi, Tomoki Furuya, Takashi Otani and Takao Saito doi:10.1016/j.tet.2008.07.102
  • Synthesis of a Potent Antimalarial Amphilectene Sergey V. Pronin and Ryan A. Shenvi Journal of the American Chemical Society 2012 134 (48), 19604-19606 doi:10.1021/ja310129b
  • Green, N. J.; Lawrence, A. L.; Bojase, G.; Willis, A. C.; Paddon-Row, M. N.; Sherburn, M. S. (2013). "Domino Cycloaddition Organocascades of Dendralenes". Angew. Chem. Int. Ed. 52 (32): 8333–8336. doi:10.1002/anie.201302185. PMID 23804245.
  • Practical Synthesis and Reactivity of [3]Dendralene Tanya A. Bradford, Alan D. Payne, Anthony C. Willis, Michael N. Paddon-Row, and Michael S. Sherburn The Journal of Organic Chemistry 2010 75 (2), 491-494 doi:10.1021/jo9024557
  • Multicomponent Diene-Transmissive Diels–Alder Sequences Featuring Aminodendralenes S. M. Tan, A. C. Willis, M. N. Paddon-Row, M. S. Sherburn, Angew. Chem. Int. Ed. 2016, 55, 3081. doi:10.1002/anie.201510925
  • Synthesis and Diels–Alder Reactivity of Substituted [4]Dendralenes Mehmet F. Saglam, Ali R. Alborzi, Alan D. Payne, Anthony C. Willis, Michael N. Paddon-Row, and Michael S. Sherburn The Journal of Organic Chemistry 2016 81 (4), 1461-1475 doi:10.1021/acs.joc.5b02583
  • Bojase, Gomotsang; Nguyen, Thanh V.; Payne, Alan D.; Willis, Anthony C.; Sherburn, Michael S. (2011). "Synthesis and properties of the ivyanes: the parent 1,1-oligocyclopropanes" (PDF). Chem. Sci. 2 (2): 229–232. doi:10.1039/C0SC00500B. hdl:1885/58011.
  • Tetrahedron Letters Volume 35, Issue 29, 18 July 1994, Pages 5251–5252 A novel photochemical reaction of [3]dendralene derivatives Keiji Okada, Katsuji Maehara, Masaji Oda doi:10.1016/S0040-4039(00)77076-6
  • Transformation of azulenes to bicyclic [4]dendralene and heptafulvene derivatives via photochemical cycloaddition of dialkylsilylene Tomoyuki Kosai, Shintaro Ishida ,Takeaki Iwamoto Chem. Commun., 2015,51, 10707-10709 doi:10.1039/C5CC03424H

handle.net (Global: 102nd place; English: 76th place)

hdl.handle.net

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

pubmed.ncbi.nlm.nih.gov

  • Hopf, H.; Sherburn, M. S. (2012). "Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular Complexity". Angewandte Chemie International Edition in English. 51 (10): 2298–2338. doi:10.1002/anie.201102987. PMID 22337341.
  • Bradford, Tanya A.; Payne, Alan D.; Willis, Anthony C.; Paddon-Row, Michael N.; Sherburn, Michael S. (2007). "Cross-Coupling for Cross-Conjugation:? Practical Synthesis and Diels?Alder Reactions of [3]Dendralenes". Organic Letters. 9 (23): 4861–4864. doi:10.1021/ol7021998. PMID 17929828.
  • Payne, Alan D.; Willis, Anthony C.; Sherburn, Michael S. (2005). "Practical Synthesis and Diels−Alder Chemistry of [4]Dendralene". Journal of the American Chemical Society. 127 (35): 12188–12189. doi:10.1021/ja053772+. ISSN 0002-7863. PMID 16131173.
  • Green, N. J.; Lawrence, A. L.; Bojase, G.; Willis, A. C.; Paddon-Row, M. N.; Sherburn, M. S. (2013). "Domino Cycloaddition Organocascades of Dendralenes". Angew. Chem. Int. Ed. 52 (32): 8333–8336. doi:10.1002/anie.201302185. PMID 23804245.

worldcat.org (Global: 5th place; English: 5th place)

search.worldcat.org

  • Payne, Alan D.; Willis, Anthony C.; Sherburn, Michael S. (2005). "Practical Synthesis and Diels−Alder Chemistry of [4]Dendralene". Journal of the American Chemical Society. 127 (35): 12188–12189. doi:10.1021/ja053772+. ISSN 0002-7863. PMID 16131173.