Indene (English Wikipedia)

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

Last modified: 14:12:52, 3 September 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

77doi.org

2^nd place

41cdc.gov

251^st place

248^th place

11wisc.edu

891^st place

533^rd place

11web.archive.org

1^st place

11arxiv.org

49^th place

31^st place

11acs.org

865^th place

887^th place

11orgsyn.org

3,535^th place

4,321^st place

acs.org (Global: 865^th place; English: 887^th place)

pubs.acs.org

Yasuda, M., Kojima, R., Tsutsui, H., Utsunomiya, D., Ishii, K., Jinnouchi, K., Shiragami, T., Yamashita, T. (1 October 2003). "Redox-Photosensitized Aminations of 1,2-Benzo-1,3-cycloalkadienes, Arylcyclopropanes, and Quadricyclane with Ammonia". The Journal of Organic Chemistry. 68 (20): 7618–7624. doi:10.1021/jo030053+.

arxiv.org (Global: 49^th place; English: 31^st place)

Haid, S.; Gugeler, K.; Kästner, J.; Campisi, D. (2025). "Superhydrogenation of indene at low temperatures". Astronomy & Astrophysics. 701: A34. arXiv:2507.22036. doi:10.1051/0004-6361/202451572.

cdc.gov (Global: 251^st place; English: 248^th place)

NIOSH Pocket Guide to Chemical Hazards. "#0340". National Institute for Occupational Safety and Health (NIOSH).

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

International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 207. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
Bordwell FG (1988). "Equilibrium acidities in dimethyl sulfoxide solution". Accounts of Chemical Research. 21 (12): 456–463. doi:10.1021/ar00156a004. Bordwell pKa Table in DMSO Archived 2008-10-09 at the Wayback Machine
Wu, Jie; Qiu, Guanyinsheng (2014). "Generation of Indene Derivatives by Tandem Reactions". Synlett. 25 (19): 2703–2713. doi:10.1055/s-0034-1379318.
O'Connor, Joseph M.; Casey, Charles P. (1987). "Ring-Slippage Chemistry of Transition Metal Cyclopentadienyl and Indenyl Complexes". Chemical Reviews. 87 (2): 307–318. doi:10.1021/cr00078a002.
Haid, S.; Gugeler, K.; Kästner, J.; Campisi, D. (2025). "Superhydrogenation of indene at low temperatures". Astronomy & Astrophysics. 701: A34. arXiv:2507.22036. doi:10.1051/0004-6361/202451572.
Yasuda, M., Kojima, R., Tsutsui, H., Utsunomiya, D., Ishii, K., Jinnouchi, K., Shiragami, T., Yamashita, T. (1 October 2003). "Redox-Photosensitized Aminations of 1,2-Benzo-1,3-cycloalkadienes, Arylcyclopropanes, and Quadricyclane with Ammonia". The Journal of Organic Chemistry. 68 (20): 7618–7624. doi:10.1021/jo030053+.
"2-INDANONE". Organic Syntheses. 41: 53. 1961. doi:10.15227/orgsyn.041.0053.

orgsyn.org (Global: 3,535^th place; English: 4,321^st place)

"2-INDANONE". Organic Syntheses. 41: 53. 1961. doi:10.15227/orgsyn.041.0053.

web.archive.org (Global: 1^st place; English: 1^st place)

Bordwell FG (1988). "Equilibrium acidities in dimethyl sulfoxide solution". Accounts of Chemical Research. 21 (12): 456–463. doi:10.1021/ar00156a004. Bordwell pKa Table in DMSO Archived 2008-10-09 at the Wayback Machine

wisc.edu (Global: 891^st place; English: 533^rd place)

chem.wisc.edu

Bordwell FG (1988). "Equilibrium acidities in dimethyl sulfoxide solution". Accounts of Chemical Research. 21 (12): 456–463. doi:10.1021/ar00156a004. Bordwell pKa Table in DMSO Archived 2008-10-09 at the Wayback Machine

Indene (English Wikipedia)

acs.org (Global: 865th place; English: 887th place)

pubs.acs.org

arxiv.org (Global: 49th place; English: 31st place)

cdc.gov (Global: 251st place; English: 248th place)

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

orgsyn.org (Global: 3,535th place; English: 4,321st place)

web.archive.org (Global: 1st place; English: 1st place)

wisc.edu (Global: 891st place; English: 533rd place)