Indol (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Indol" in Galician language version.

Last modified: 20:12:04, 25 September 2024 (UTC)

Ref.Un. Ref.Website

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1616doi.org

2^nd place

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33nih.gov

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22orgsyn.org

3,535^th place

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22acs.org

865^th place

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11worldcat.org

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11leffingwell.com

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5,359^th place

11wiley.com

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acs.org (Global: 865^th place; Galician: 366^th place)

pubs.acs.org

Alan R. Katritzky, Jianqing Li, Christian V. Stevens (1995). "Facile Synthesis of 2-Substituted Indoles and Indolo[3,2-b]carbazoles from 2-(Benzotriazol-1-ylmethyl)indole". J. Org. Chem. 60 (11): 3401–3404. doi:10.1021/jo00116a026.
Cox, E. D.; Cook, J. M. (1995). "The Pictet-Spengler condensation: a new direction for an old reaction". Chemical Reviews 95 (6): 1797–1842. doi:10.1021/cr00038a004.

doi.org (Global: 2^nd place; Galician: 3^rd place)

dx.doi.org

Lee, Jin-Hyung; Lee, Jintae (2010). "Indole as an intercellular signal in microbial communities". FEMS Microbiology Reviews. ISSN 0168-6445. doi:10.1111/j.1574-6976.2009.00204.x.
Baeyer, A. (1866). "Ueber die Reduction aromatischer Verbindungen mittelst Zinkstaub". Ann. 140 (3): 295. doi:10.1002/jlac.18661400306.
Baeyer, A.; Emmerling, A. (1869). "Synthese des Indols". Chemische Berichte 2: 679. doi:10.1002/cber.186900201268.
R. B. Van Order, H. G. Lindwall (1942). "Indole". Chem. Rev. 30: 69–96. doi:10.1021/cr60095a004.
Gribble G. W. (2000). "Recent developments in indole ring synthesis—methodology and applications". J. Chem. Soc. Perkin Trans. 1 (7): 1045. doi:10.1039/a909834h.
Cacchi, S.; Fabrizi, G. (2005). "Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions". Chem. Rev. 105 (7): 2873. PMID 16011327. doi:10.1021/cr040639b.
Humphrey, G. R.; Kuethe, J. T. (2006). "Practical Methodologies for the Synthesis of Indoles". Chem. Rev. 106 (7): 2875. PMID 16836303. doi:10.1021/cr0505270.
Bratulescu, George (2008). "A new and efficient one-pot synthesis of indoles". Tetrahedron Letters 49 (6): 984. doi:10.1016/j.tetlet.2007.12.015.
Diels, Otto; Reese, Johannes (1934). "Synthesen in der hydroaromatischen Reihe. XX. Über die Anlagerung von Acetylen-dicarbonsäureester an Hydrazobenzol". Ann. 511: 168. doi:10.1002/jlac.19345110114.
Ernest H. Huntress, Joseph Bornstein, and William M. Hearon (1956). "An Extension of the Diels-Reese Reaction". J. Am. Chem. Soc. 78 (10): 2225. doi:10.1021/ja01591a055.
Bergman, J.; Venemalm, L. (1992). "Efficient synthesis of 2-chloro-, 2-bromo-, and 2-iodoindole". J. Org. Chem. 57 (8): 2495. doi:10.1021/jo00034a058.
Alan R. Katritzky, Jianqing Li, Christian V. Stevens (1995). "Facile Synthesis of 2-Substituted Indoles and Indolo[3,2-b]carbazoles from 2-(Benzotriazol-1-ylmethyl)indole". J. Org. Chem. 60 (11): 3401–3404. doi:10.1021/jo00116a026.
Lynch, S. M. ; Bur, S. K.; Padwa, A. (2002). "Intramolecular Amidofuran Cycloadditions across an Indole π-Bond: An Efficient Approach to the Aspidosperma and Strychnos ABCE Core". Org. Lett. 4 (26): 4643. PMID 12489950. doi:10.1021/ol027024q.
Gremmen, C.; Willemse, B.; Wanner, M. J.; Koomen, G.-J. (2000). "Enantiopure Tetrahydro-β-carbolines via Pictet-Spengler Reactions with N-Sulfinyl Tryptamines". Org. Lett. 2 (13): 1955–1958. doi:10.1021/ol006034t.
Larghi, Enrique L.; Amongero, Marcela; Bracca, Andrea B. J.; Kaufman, Teodoro S. (2005-10-07). "The intermolecular Pictet-Spengler condensation with chiral carbonyl derivatives in the stereoselective syntheses of optically-active isoquinoline and indole alkaloids". ARKIVOC. Commemorative Issue in Honor of Prof. Rosa Lederkremer on the occasion of her 70th anniversary (2005-10-19) 2005 (12): 98–153. doi:10.3998/ark.5550190.0006.c09.
Bonnet, D.; Ganesan, A. (2002). "Solid-Phase Synthesis of Tetrahydro-β-carbolinehydantoins via the N-Acyliminium Pictet-Spengler Reaction and Cyclative Cleavage". J. Comb. Chem. 4 (6): 546–548. doi:10.1021/cc020026h.

leffingwell.com (Global: low place; Galician: 5,359^th place)

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

nih.gov (Global: 5^th place; Galician: 2^nd place)

ncbi.nlm.nih.gov

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

orgsyn.org (Global: 3,535^th place; Galician: 592^nd place)

James, P. N.; Snyder, H. R. (1959). "Indole-3-aldehyde". Organic Syntheses 39: 30.
Heaney, H.; Ley, S. V. (1974). "1-Benzylindole". Organic Syntheses 54: 58.

wiley.com (Global: 150^th place; Galician: 77^th place)

onlinelibrary.wiley.com

Gerd Collin and Hartmut Höke “Indole” Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. DOI 10.1002/14356007.a14_167 .

worldcat.org (Global: 4^th place; Galician: 7^th place)

Lee, Jin-Hyung; Lee, Jintae (2010). "Indole as an intercellular signal in microbial communities". FEMS Microbiology Reviews. ISSN 0168-6445. doi:10.1111/j.1574-6976.2009.00204.x.

Indol (Galician Wikipedia)

acs.org (Global: 865th place; Galician: 366th place)

pubs.acs.org

doi.org (Global: 2nd place; Galician: 3rd place)

dx.doi.org

leffingwell.com (Global: low place; Galician: 5,359th place)

nih.gov (Global: 5th place; Galician: 2nd place)