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Hexadehydro Diels–Alder reaction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hexadehydro Diels–Alder reaction" in English language version.

refsWebsite
Global rank English rank
12doi.org
2nd place
2nd place
6nih.gov
4th place
4th place
4sciencedirect.com
149th place
178th place
3worldcat.org
5th place
5th place
2rsc.org
2,020th place
1,872nd place
1wiley.com
222nd place
297th place
1csiro.au
4,114th place
3,147th place
1heterocycles.jp
low place
low place
1jst.go.jp
1,903rd place
2,346th place
1acs.org
1,248th place
1,104th place
1harvard.edu
18th place
17th place

acs.org

pubs.acs.org

  • Niu, D.; Wang, T.; Woods, B. P.; Hoye, T. R. Org. Lett., 2014, 16, 254 [17]

csiro.au

publish.csiro.au

  • Cahill, K. J.; Ajaz, A.; Johnson, R. P. Aust. J. Chem., 2010, 63, 1007 [8]

doi.org

dx.doi.org

  • Hoye, T. R.; Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P. Nature, 2012, 490, 208 [1]
  • Yeoman, J. T. S.; Reisman, S. E. Nature, 2012, 490, 179
  • Yun, S. Y.; Wang, K.-P.; Lee, N.-K.; Mamidipalli, P.; Lee, D. J. Am. Chem. Soc., 2013, 135, 4668 [3]
  • Ajaz, A.; Bradley, A. Z.; Burrell, R. C.; Li, W. H. H.; Daoust, K. J.; Bovee, L. B.; DiRico, K. J.; Johnson, R. P. J. Org. Chem., 2011, 76, 9320 [5]
  • Liang, Y.; Hong, X.; Yu, P.; Houk, K. N. Org. Lett., 2014, 16, 5702 [6]
  • Bradley, A. Z.; Johnson, R. P. J. Am. Chem. Soc., 1997, 119, 9917 [7]
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  • Niu, D.; Hoye, T. R. Nat. Chem., 2014, 6, 34
  • Niu, D.; Willoughby, P. H.; Woods, B. P.; Baire, B.; Hoye, T. R. Nature, 2013, 501, 531 [18]

doi.org

  • Xiao, Xiao; Hoye, Thomas R. (2018-07-20). "The domino hexadehydro-Diels–Alder reaction transforms polyynes to benzynes to naphthynes to anthracynes to tetracynes (and beyond?)". Nature Chemistry. 10 (8): 838–844. Bibcode:2018NatCh..10..838X. doi:10.1038/s41557-018-0075-y. ISSN 1755-4349. PMC 6284823. PMID 30030536.
  • Thompson, Severin K.; Hoye, Thomas R. (2019-12-01). "The Aza-hexadehydro-Diels–Alder Reaction". Journal of the American Chemical Society. 141 (50): 19575–19580. doi:10.1021/jacs.9b11243. ISSN 0002-7863. PMC 6921493. PMID 31789026.
  • Lee, Daniel; Ross, Sean P.; Xiao, Xiao; Hoye, Thomas R. (2021-09-09). "Radial hexadehydro-Diels-Alder reactions". Chem. 7 (9): 2527–2537. doi:10.1016/j.chempr.2021.08.010. ISSN 2451-9294. PMC 8797013. PMID 35097238.

harvard.edu

ui.adsabs.harvard.edu

  • Xiao, Xiao; Hoye, Thomas R. (2018-07-20). "The domino hexadehydro-Diels–Alder reaction transforms polyynes to benzynes to naphthynes to anthracynes to tetracynes (and beyond?)". Nature Chemistry. 10 (8): 838–844. Bibcode:2018NatCh..10..838X. doi:10.1038/s41557-018-0075-y. ISSN 1755-4349. PMC 6284823. PMID 30030536.

heterocycles.jp

  • K. Miyawaki, F. Ueno, I. Ueda, Heterocycles, 2001, 54, 887 [12]

jst.go.jp

jstage.jst.go.jp

nih.gov

ncbi.nlm.nih.gov

  • Xiao, Xiao; Hoye, Thomas R. (2018-07-20). "The domino hexadehydro-Diels–Alder reaction transforms polyynes to benzynes to naphthynes to anthracynes to tetracynes (and beyond?)". Nature Chemistry. 10 (8): 838–844. Bibcode:2018NatCh..10..838X. doi:10.1038/s41557-018-0075-y. ISSN 1755-4349. PMC 6284823. PMID 30030536.
  • Thompson, Severin K.; Hoye, Thomas R. (2019-12-01). "The Aza-hexadehydro-Diels–Alder Reaction". Journal of the American Chemical Society. 141 (50): 19575–19580. doi:10.1021/jacs.9b11243. ISSN 0002-7863. PMC 6921493. PMID 31789026.
  • Lee, Daniel; Ross, Sean P.; Xiao, Xiao; Hoye, Thomas R. (2021-09-09). "Radial hexadehydro-Diels-Alder reactions". Chem. 7 (9): 2527–2537. doi:10.1016/j.chempr.2021.08.010. ISSN 2451-9294. PMC 8797013. PMID 35097238.

pubmed.ncbi.nlm.nih.gov

  • Xiao, Xiao; Hoye, Thomas R. (2018-07-20). "The domino hexadehydro-Diels–Alder reaction transforms polyynes to benzynes to naphthynes to anthracynes to tetracynes (and beyond?)". Nature Chemistry. 10 (8): 838–844. Bibcode:2018NatCh..10..838X. doi:10.1038/s41557-018-0075-y. ISSN 1755-4349. PMC 6284823. PMID 30030536.
  • Thompson, Severin K.; Hoye, Thomas R. (2019-12-01). "The Aza-hexadehydro-Diels–Alder Reaction". Journal of the American Chemical Society. 141 (50): 19575–19580. doi:10.1021/jacs.9b11243. ISSN 0002-7863. PMC 6921493. PMID 31789026.
  • Lee, Daniel; Ross, Sean P.; Xiao, Xiao; Hoye, Thomas R. (2021-09-09). "Radial hexadehydro-Diels-Alder reactions". Chem. 7 (9): 2527–2537. doi:10.1016/j.chempr.2021.08.010. ISSN 2451-9294. PMC 8797013. PMID 35097238.

rsc.org

pubs.rsc.org

  • Vandavasi, J. K.; Hu, W.-P.; Hsiao, C.-T.; Senadi, G. C.; Wang, J.-J. RSC Adv., 2014, 4, 57547 [4]
  • Wang, K.-P.; Yun, S. Y.; Mamidipalli, P.; Lee, D. Chem. Sci., 2013, 4, 3205 [16]

sciencedirect.com

  • Miyawaki, K.; Suzuki, R.; Kawano, T.; Ueda, I. Tetrahedron Lett., 1997, 38, 3943 [9]
  • Ueda, I.; Sakurai, Y.; Kawano, T.; Wada, Y.; Futai, M. Tetrahedron Lett., 1999, 40, 319 [10]
  • Miyawaki, K.; Kawano, T.; Ueda, I. Tetrahedron Lett., 2000, 41, 1447 [11]
  • Torikai, K.; Otsuka, Y.; Nishimura, M.; Sumida, M.; Kawai, T.; Sekiguchi, K.; Ueda, I. Bioorg. Med. Chem., 2008, 16, 5441 [13]

wiley.com

onlinelibrary.wiley.com

  • Holden, C.; Greaney, M. F. Angew. Chem. Int. Ed. Engl., 2014, 53, 5746 [2]

worldcat.org

search.worldcat.org

  • Xiao, Xiao; Hoye, Thomas R. (2018-07-20). "The domino hexadehydro-Diels–Alder reaction transforms polyynes to benzynes to naphthynes to anthracynes to tetracynes (and beyond?)". Nature Chemistry. 10 (8): 838–844. Bibcode:2018NatCh..10..838X. doi:10.1038/s41557-018-0075-y. ISSN 1755-4349. PMC 6284823. PMID 30030536.
  • Thompson, Severin K.; Hoye, Thomas R. (2019-12-01). "The Aza-hexadehydro-Diels–Alder Reaction". Journal of the American Chemical Society. 141 (50): 19575–19580. doi:10.1021/jacs.9b11243. ISSN 0002-7863. PMC 6921493. PMID 31789026.
  • Lee, Daniel; Ross, Sean P.; Xiao, Xiao; Hoye, Thomas R. (2021-09-09). "Radial hexadehydro-Diels-Alder reactions". Chem. 7 (9): 2527–2537. doi:10.1016/j.chempr.2021.08.010. ISSN 2451-9294. PMC 8797013. PMID 35097238.