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1-四氢萘酮 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "1-四氢萘酮" in Chinese language version.

refsWebsite
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20doi.org
2nd place
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2web.archive.org
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1st place
2nih.gov
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2espacenet.com
800th place
1,214th place
1sigmaaldrich.com
924th place
1,167th place
1tcichemicals.com
low place
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1epfl.ch
4,521st place
2,540th place
1worldcat.org
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doi.org (Global: 2nd place; Chinese: 23rd place)

  • H.R. Snyder, F.X. Werber. α-Tetralone. Org. Synth. 1940, 20: 94. doi:10.15227/orgsyn.020.0094. 
  • P.-C. Kuo; Y.-C. Li; T.-S. Wu, Chemical constituents and pharmacology of the Aristolochia species, EJTCM 2 (4), 2012, 2 (4): 249–266, PMC 3942903 可免费查阅, PMID 24716140, doi:10.1016/S2225-4110(16)30111-0 可免费查阅 
  • H. Hock; W. Susemihl, Autoxydation von Kohlenwasserstoffen: Über ein durch Autoxydation erhaltenes Tetrahydro-naphthalin-peroxyd (I. Mitteil.), 德国化学学报 66 (1), 1933, 66 (1): 61–68, doi:10.1002/cber.19330660113 （德语） 
  • S. Bhattacharjee; Y.-R. Lee; W.-S. Ahn, Oxidation of tetraline to 1-tetralone over CrAPO-5, Korean J. Chem. Eng. 34 (3), 2017, 34 (3): 701–705, doi:10.1007/s11814-016-0310-4 （德语） 
  • C.E. Olson, A.R. Bader. α-Tetralone. Org. Synth. 1955, 35: 95. doi:10.15227/orgsyn.035.0095. 
  • L. F. Somerville, C. F. H. Allen. β-Benzoylpropionic acid. Org. Synth. 1933, 13: 12. doi:10.15227/orgsyn.013.0012. 
  • V. Premasagar; V.A. Palaniswamy; E.J. Eisenbraun, Methanesulfonic acid catalyzed cyclization of 3-arylpropanoic and 4-arylbutanoic acids to 1-indanones and 1-tetralones, 有机化学期刊 46 (14), 1981, 46 (14): 2974–2976, doi:10.1021/jo00325a028 
  • M.S. Holden; R.D. Crouch; K.A. Barker, Formation of α-tetralone by intramolecular Friedel-Crafts acylation, J. Chem. Educ. 82 (6), 2005, 82 (6): 934–935, doi:10.1021/ed082p934 
  • S. Antoniotti; E. Dunach, Facile preparation of metallic triflates and triflimidates by oxidative dissolution of metal powders, Chem. Commun. 8 (8), 2008, 8 (8): 993–995, doi:10.1039/B717689A 
  • D.-M. Cui; M. Kawamura; S. Shimada; T. Hayashi; M. Tanaka, Synthesis of 1-tetralones by intramolecular Friedel-Crafts reaction of 4-arylbutyric acids using Lewis acid catalysts, 四面体通讯 44 (21), 2003, 44 (21): 4007–4010, doi:10.1016/S0040-4039(03)00855-4 
  • H. Motiwala; R.H. Vekariya; J. Aubé, Intramolecular Friedel-Crafts acylation reaction promoted by 1,1,1,3,3,3-hexafluoro-2-propanol, 有机化学通讯 17 (21), 2015, 17 (21): 5484–5487, PMID 26496158, doi:10.1021/acs.orglett.5b02851 （德语） 
  • S.S. Hall; S.D. Lipsky; F.J. McEnroe; A.P. Bartels, Lithium-ammonia Reduction of Aromatic Ketones to Aromatic Hydrocarbons, 有机化学期刊 38 (18), 1971, 38 (18): 2588–2591, doi:10.1021/jo00817a004 
  • Z. Marcinow; P.W. Rabideau, Metal-Ammonia Reduction of α-Tetralone. Competition Between Ring Reduction, Carbonyl Reduction, and Dimer Formation, 有机化学期刊 53 (9), 1988, 53 (9): 2117–2119, doi:10.1021/jo00244a054 
  • J.R. Hwu; Y.S. Wein; Y.-J. Leu, Calcium metal in liquid ammonia for selective reduction of organic compounds, 有机化学期刊 61 (4), 1996, 61 (4): 1493–1499, doi:10.1021/jo951219c （德语） 
  • Methylene ketones and aldehydes by simple, direct methylene transfer: 2-Methylene-1-oxo-1,2,3,4-tetrahydronaphthalene. Organic Syntheses. 1981, 60: 88. doi:10.15227/orgsyn.060.0088. 
  • I. Yuranov; L. Kiwi-Minsker; A. Renken, One-step vapour-phase synthesis of 2-methyl-1-naphthol from 1-tetralone, Appl. Catal. A 226 (1–2), 2002, 226 (1–2): 193–198 [2021-11-08], doi:10.1016/S0926-860X(01)00902-4, （原始内容存档于2021-11-08） （德语） 
  • M.S. Newman; W.M. Hung, An improved aromatization of α-tetralone oximes to N-(1-naphthyl)acetamides, 有机化学期刊 38 (23), 1973, 38 (23): 4073–4074, doi:10.1021/jo00987a029 （德语） 
  • 1-Phenylnaphthalene. Organic Syntheses. 1944, 24: 84. doi:10.15227/orgsyn.024.0084. 
  • G.P. Kantin; M. Krasavin, Reaction of α-tetralone, 1H-tetrazol-5-amine, and aromatic aldehydes upon microwave irradiation – a convenient method for the synthesis of 5,6,7,12-tetrahydrobenzo[h]tetrazolo[5,1-b]quinazolines, Chem. Heterocycl. Compd. 52 (11), 2016, 52 (11): 918–922, doi:10.1007/s10593-017-1985-0 （德语） 
  • Kaiser, Carl; Jen, Timothy; Garvey, Eleanor; Bowen, Wayne D.; Colella, Donald F.; Wardell, Joe R. Adrenergic agents. 4. Substituted phenoxypropanolamine derivatives as potential .beta.-adrenergic agonists. Journal of Medicinal Chemistry (American Chemical Society (ACS)). 1977, 20 (5): 687–692. ISSN 0022-2623. doi:10.1021/jm00215a014. 

epfl.ch (Global: 4,521st place; Chinese: 2,540th place)

infoscience.epfl.ch

espacenet.com (Global: 800th place; Chinese: 1,214th place)

worldwide.espacenet.com

  • US 4473711,R.W. Coon,「Liquid-phase process for oxidation of tetralin」,发表于1984-09-25 
  • DE 2421745,K. Kudo, T. Ohmae, A. Uno,「Verfahren zur Herstellung von α-Naphthol durch katalytische Dehydrierung von α-Tetralon」,发表于1975-11-20 

nih.gov (Global: 4th place; Chinese: 5th place)

ncbi.nlm.nih.gov

sigmaaldrich.com (Global: 924th place; Chinese: 1,167th place)

  • 来源：Sigma-Aldrich Co., α-Tetralon （25. November 2017查阅）.

tcichemicals.com (Global: low place; Chinese: low place)

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

worldcat.org (Global: 5th place; Chinese: 12th place)

  • Kaiser, Carl; Jen, Timothy; Garvey, Eleanor; Bowen, Wayne D.; Colella, Donald F.; Wardell, Joe R. Adrenergic agents. 4. Substituted phenoxypropanolamine derivatives as potential .beta.-adrenergic agonists. Journal of Medicinal Chemistry (American Chemical Society (ACS)). 1977, 20 (5): 687–692. ISSN 0022-2623. doi:10.1021/jm00215a014.