傅里德-克拉夫茨反应 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "傅里德-克拉夫茨反应" in Chinese language version.

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archive.org

K. Wallace, R. Hanes, E. Anslyn, J. Morey, K. Kilway and J. Siegel. Preparation of 1,3,5-Tris(aminomethyl)-2,4,6-triethylbenzene from Two Versatile 1,3,5-Tri(halosubstituted) 2,4,6-Triethylbenzene Derivatives. Synthesis. 2005, 2005 (12): 2080–2083. doi:10.1055/s-2005-869963.

bnf.fr

gallica.bnf.fr

Friedel, C.; Crafts, J. M. Compt. Rend. 1877, 84, 1392 （页面存档备份，存于互联网档案馆） & 1450 （页面存档备份，存于互联网档案馆）.

books.google.com

Li, Jie Jack (2003) Name Reactions: A Collection of Detailed Reaction Mechanisms （页面存档备份，存于互联网档案馆）, Springer, ISBN 3-540-40203-9, p. 175.

doi.org

Groves, J. K. The Friedel–Crafts acylation of alkenes. Chem. Soc. Rev. 1972, 1: 73. doi:10.1039/cs9720100073.
S. Hajra, B. Maji and S. Bar. Samarium Triflate-Catalyzed Halogen-Promoted Friedel–Crafts Alkylation with Alkenes. Org. Lett. 2007, 9 (15): 2783–2786. doi:10.1021/ol070813t.
K. Wallace, R. Hanes, E. Anslyn, J. Morey, K. Kilway and J. Siegel. Preparation of 1,3,5-Tris(aminomethyl)-2,4,6-triethylbenzene from Two Versatile 1,3,5-Tri(halosubstituted) 2,4,6-Triethylbenzene Derivatives. Synthesis. 2005, 2005 (12): 2080–2083. doi:10.1055/s-2005-869963.
R. C. Fuson, H. H. Weinstock and G. E. Ullyot. A New Synthesis of Benzoins. 2′,4′,6′-Trimethylbenzoin. J. Am. Chem. Soc. 1935, 57 (10): 1803–1804. doi:10.1021/ja01313a015.
This reaction withphosphorus pentoxide: J. v. d. Kamp and E. Mosettig. Trans- And Cis-As-Octahydrophenanthrene. J. Am. Chem. Soc. 1936, 58 (6): 1062–1063. doi:10.1021/ja01297a514.
Sereda, Grigoriy A.; Rajpara, Vikul B. A Green Alternative to Aluminum Chloride Alkylation of Xylene. J. Chem. Educ. 2007, 2007 (84): 692 [2011-02-21]. doi:10.1021/ed084p692. （原始内容存档于2009-07-18）.
Robert Downs Haworth. Syntheses of alkylphenanthrenes. Part I. 1-, 2-, 3-, and 4-Methylphenanthrenes. J. Chem. Soc. 1932: 1125. doi:10.1039/JR9320001125.

drugfuture.com

Darzens-Nenitzescu Synthesis of Ketones. [2011-02-21]. （原始内容存档于2019-06-20）.
Nenitzescu Reductive Acylation. [2011-02-21]. （原始内容存档于2018-10-02）.

orgsyn.org

W. T. Smith, Jr. and J. T. Sellas (1963). "Neophyl chloride". Org. Synth..

web.archive.org

Friedel, C.; Crafts, J. M. Compt. Rend. 1877, 84, 1392 （页面存档备份，存于互联网档案馆） & 1450 （页面存档备份，存于互联网档案馆）.
Darzens-Nenitzescu Synthesis of Ketones. [2011-02-21]. （原始内容存档于2019-06-20）.
Nenitzescu Reductive Acylation. [2011-02-21]. （原始内容存档于2018-10-02）.
Sereda, Grigoriy A.; Rajpara, Vikul B. A Green Alternative to Aluminum Chloride Alkylation of Xylene. J. Chem. Educ. 2007, 2007 (84): 692 [2011-02-21]. doi:10.1021/ed084p692. （原始内容存档于2009-07-18）.
McCullagh, James V.; Daggett, Kelly A. Synthesis of Triarylmethane and Xanthene Dyes Using Electrophilic Aromatic Substitution Reactions. J. Chem. Educ. 2007, 84: 1799 [2011-02-21]. （原始内容存档于2008-06-13）.
Li, Jie Jack (2003) Name Reactions: A Collection of Detailed Reaction Mechanisms （页面存档备份，存于互联网档案馆）, Springer, ISBN 3-540-40203-9, p. 175.

wisc.edu

jchemed.chem.wisc.edu

Sereda, Grigoriy A.; Rajpara, Vikul B. A Green Alternative to Aluminum Chloride Alkylation of Xylene. J. Chem. Educ. 2007, 2007 (84): 692 [2011-02-21]. doi:10.1021/ed084p692. （原始内容存档于2009-07-18）.
McCullagh, James V.; Daggett, Kelly A. Synthesis of Triarylmethane and Xanthene Dyes Using Electrophilic Aromatic Substitution Reactions. J. Chem. Educ. 2007, 84: 1799 [2011-02-21]. （原始内容存档于2008-06-13）.