吲哚 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "吲哚" in Chinese language version.

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Alan R. Katritzky, Jianqing Li, Christian V. Stevens. Facile Synthesis of 2-Substituted Indoles and Indolo[3,2-b]carbazoles from 2-(Benzotriazol-1-ylmethyl)indole. J. Org. Chem. 1995, 60 (11): 3401–3404 [2011-06-27]. doi:10.1021/jo00116a026. （原始内容存档于2020-03-16）.

doi.org

Baeyer, A. Ueber die Reduction aromatischer Verbindungen mittelst Zinkstaub. Ann. 1866, 140 (3): 295. doi:10.1002/jlac.18661400306.
Baeyer, A.; Emmerling, A. Synthese des Indols. Chemische Berichte. 1869, 2: 679. doi:10.1002/cber.186900201268.
R. B. Van Order, H. G. Lindwall. Indole. Chem. Rev. 1942, 30: 69–96. doi:10.1021/cr60095a004.
Gribble G. W. Recent developments in indole ring synthesis—methodology and applications. J. Chem. Soc. Perkin Trans. 1（英语：J. Chem. Soc. Perkin Trans. 1）. 2000, (7): 1045. doi:10.1039/a909834h.
Cacchi, S.; Fabrizi, G. Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions. Chem. Rev. 2005, 105 (7): 2873. PMID 16011327. doi:10.1021/cr040639b.
Humphrey, G. R.; Kuethe, J. T. Practical Methodologies for the Synthesis of Indoles. Chem. Rev. 2006, 106 (7): 2875. PMID 16836303. doi:10.1021/cr0505270.
Gerd Collin and Hartmut Höke “Indole” Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. doi:10.1002/14356007.a14_167.
Bergman, J.; Venemalm, L. Efficient synthesis of 2-chloro-, 2-bromo-, and 2-iodoindole. J. Org. Chem. 1992, 57 (8): 2495. doi:10.1021/jo00034a058.
Alan R. Katritzky, Jianqing Li, Christian V. Stevens. Facile Synthesis of 2-Substituted Indoles and Indolo[3,2-b]carbazoles from 2-(Benzotriazol-1-ylmethyl)indole. J. Org. Chem. 1995, 60 (11): 3401–3404 [2011-06-27]. doi:10.1021/jo00116a026. （原始内容存档于2020-03-16）.
Lynch, S. M. ; Bur, S. K.; Padwa, A. Intramolecular Amidofuran Cycloadditions across an Indole π-Bond: An Efficient Approach to the Aspidosperma and Strychnos ABCE Core. Org. Lett. 2002, 4 (26): 4643. PMID 12489950. doi:10.1021/ol027024q.

leffingwell.com

http://www.leffingwell.com/olfact5.htm

nih.gov

ncbi.nlm.nih.gov

Cacchi, S.; Fabrizi, G. Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions. Chem. Rev. 2005, 105 (7): 2873. PMID 16011327. doi:10.1021/cr040639b.
Humphrey, G. R.; Kuethe, J. T. Practical Methodologies for the Synthesis of Indoles. Chem. Rev. 2006, 106 (7): 2875. PMID 16836303. doi:10.1021/cr0505270.
Lynch, S. M. ; Bur, S. K.; Padwa, A. Intramolecular Amidofuran Cycloadditions across an Indole π-Bond: An Efficient Approach to the Aspidosperma and Strychnos ABCE Core. Org. Lett. 2002, 4 (26): 4643. PMID 12489950. doi:10.1021/ol027024q.

orgsyn.org

James, P. N.; Snyder, H. R. Indole-3-aldehyde. Organic Syntheses. 1959, 39: 30 [2011-06-27]. （原始内容存档于2012-10-02）.
Heaney, H.; Ley, S. V. 1-Benzylindole. Organic Syntheses. 1974, 54: 58 [2011-06-27]. （原始内容存档于2012-10-02）.

web.archive.org

James, P. N.; Snyder, H. R. Indole-3-aldehyde. Organic Syntheses. 1959, 39: 30 [2011-06-27]. （原始内容存档于2012-10-02）.
Heaney, H.; Ley, S. V. 1-Benzylindole. Organic Syntheses. 1974, 54: 58 [2011-06-27]. （原始内容存档于2012-10-02）.
Alan R. Katritzky, Jianqing Li, Christian V. Stevens. Facile Synthesis of 2-Substituted Indoles and Indolo[3,2-b]carbazoles from 2-(Benzotriazol-1-ylmethyl)indole. J. Org. Chem. 1995, 60 (11): 3401–3404 [2011-06-27]. doi:10.1021/jo00116a026. （原始内容存档于2020-03-16）.

wikipedia.org

en.wikipedia.org

Gribble G. W. Recent developments in indole ring synthesis—methodology and applications. J. Chem. Soc. Perkin Trans. 1（英语：J. Chem. Soc. Perkin Trans. 1）. 2000, (7): 1045. doi:10.1039/a909834h.