Indane (English Wikipedia)

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

Last modified: 08:37:06, 6 August 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

1111doi.org

2^nd place

33nih.gov

5^th place

22acs.org

865^th place

887^th place

22patents.google.com

1,154^th place

606^th place

11adsabs.harvard.edu

14^th place

9^th place

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

pubs.acs.org

Arnold, R. T.; Barnes, R. A. (June 1944). "The Jacobsen Rearrangement. VIII. 1 Cyclic Systems; Mechanism". Journal of the American Chemical Society. 66 (6): 960–964. doi:10.1021/ja01234a036. Retrieved 4 November 2025.
Howbert, J. J.; Grossman, C. S.; Crowell, T. A.; Rieder, B. J.; Harper, R. W.; Kramer, K. E.; Tao, E. V.; Aikins, J.; Poore, G. A. (September 1990). "Novel agents effective against solid tumors: the diarylsulfonylureas. Synthesis, activities, and analysis of quantitative structure-activity relationships". Journal of Medicinal Chemistry. 33 (9): 2393–2407. doi:10.1021/jm00171a013.

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

ui.adsabs.harvard.edu

Gabriele, Bartolo; Mancuso, Raffaella; Veltri, Lucia (2016). "Recent Advances in the Synthesis of Indanes and Indenes". Chemistry – A European Journal. 22 (15): 5056–5094. Bibcode:2016ChEuJ..22.5056G. doi:10.1002/chem.201503933. PMID 26788795.

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. 602. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
Karl Griesbaum, Arno Behr, Dieter Biedenkapp, Heinz-Werner Voges, Dorothea Garbe, Christian Paetz, Gerd Collin, Dieter Mayer, Hartmut Höke "Hydrocarbons" in Ullmann's Encyclopedia of Industrial Chemistry 2002 Wiley-VCH, Weinheim. doi:10.1002/14356007.a13_227
Gabriele, Bartolo; Mancuso, Raffaella; Veltri, Lucia (2016). "Recent Advances in the Synthesis of Indanes and Indenes". Chemistry – A European Journal. 22 (15): 5056–5094. Bibcode:2016ChEuJ..22.5056G. doi:10.1002/chem.201503933. PMID 26788795.
Borie, Cyril; Ackermann, Lutz; Nechab, Malek (2016). "Enantioselective syntheses of indanes: From organocatalysis to C–H functionalization". Chemical Society Reviews. 45 (5): 1368–1386. doi:10.1039/c5cs00622h. PMID 26728953.
Hong, Bor-Cherng; Sarshar, Sepehr (1999). "Recent Advances in the Synthesis of Indan Systems. A Review". Organic Preparations and Procedures International. 31: 1–86. doi:10.1080/00304949909355675.
Fiege, Helmut; Voges, Heinz-Werner; Hamamoto, Toshikazu; Umemura, Sumio; Iwata, Tadao; Miki, Hisaya; Fujita, Yasuhiro; Buysch, Hans-Josef; Garbe, Dorothea; Paulus, Wilfried (2000). "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a19_313. ISBN 978-3-527-30385-4.
"(S)-Tetrahydro-1-Methyl-3,3-Diphenyl-1H,3H-Pyrrolo-[1,2-c][1,3,2]Oxazaborole-Borane Complex". Organic Syntheses. 74: 50. 1997. doi:10.15227/orgsyn.074.0050.
Nichols, D. E; Brewster, W. K; Johnson, M. P; Oberlender, R; Riggs, R. M (1990). "Nonneurotoxic tetralin and indan analogues of 3,4-(methylenedioxy)amphetamine (MDA)". Journal of Medicinal Chemistry. 33 (2): 703–10. doi:10.1021/jm00164a037. PMID 1967651.
Arnold, R. T.; Barnes, R. A. (June 1944). "The Jacobsen Rearrangement. VIII. 1 Cyclic Systems; Mechanism". Journal of the American Chemical Society. 66 (6): 960–964. doi:10.1021/ja01234a036. Retrieved 4 November 2025.
Howbert, J. J.; Grossman, C. S.; Crowell, T. A.; Rieder, B. J.; Harper, R. W.; Kramer, K. E.; Tao, E. V.; Aikins, J.; Poore, G. A. (September 1990). "Novel agents effective against solid tumors: the diarylsulfonylureas. Synthesis, activities, and analysis of quantitative structure-activity relationships". Journal of Medicinal Chemistry. 33 (9): 2393–2407. doi:10.1021/jm00171a013.
Norman L. Allinger, James L. Coke (1960), "The Relative Stabilities of cis and trans Isomers. VII. The Hydrindanes 1,2", Journal of the American Chemical Society, vol. 82, no. 10, pp. 2553–2556, doi:10.1021/ja01495a039

nih.gov (Global: 5^th place; English: 5^th place)

pubmed.ncbi.nlm.nih.gov

Gabriele, Bartolo; Mancuso, Raffaella; Veltri, Lucia (2016). "Recent Advances in the Synthesis of Indanes and Indenes". Chemistry – A European Journal. 22 (15): 5056–5094. Bibcode:2016ChEuJ..22.5056G. doi:10.1002/chem.201503933. PMID 26788795.
Borie, Cyril; Ackermann, Lutz; Nechab, Malek (2016). "Enantioselective syntheses of indanes: From organocatalysis to C–H functionalization". Chemical Society Reviews. 45 (5): 1368–1386. doi:10.1039/c5cs00622h. PMID 26728953.
Nichols, D. E; Brewster, W. K; Johnson, M. P; Oberlender, R; Riggs, R. M (1990). "Nonneurotoxic tetralin and indan analogues of 3,4-(methylenedioxy)amphetamine (MDA)". Journal of Medicinal Chemistry. 33 (2): 703–10. doi:10.1021/jm00164a037. PMID 1967651.

patents.google.com (Global: 1,154^th place; English: 606^th place)

DE2136325 idem Alex Berg, Hans-Joachim May, U.S. patent 3,882,229 (1975 to Nordmark Werke Gmbh).
Gerald A. Poore, U.S. patent 5,116,874 (1992 to Eli Lilly And Company).

Indane (English Wikipedia)

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

pubs.acs.org

adsabs.harvard.edu (Global: 14th place; English: 9th place)