Nitrilo (Galician Wikipedia)

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

Last modified: 00:24:28, 20 August 2026 (UTC)

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2726doi.org

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

pubs.acs.org

David T. Mowry (1948). "The Preparation of Nitriles" (– ^{Scholar search}). Chemical Reviews 42 (2): 189–283. PMID 18914000. doi:10.1021/cr60132a001.
Sharwan K, Dewan, Ravinder Singh, and Anil Kumar (2006). "One pot synthesis of nitriles from aldehydes and hydroxylamine hydrochloride using sodium sulfate (anhyd) and sodium bicarbonate in dry media under microwave irradiation". Arkivoc: (ii) 41–44.

adsabs.harvard.edu (Global: 14^th place; Galician: 17^th place)

Smith, Andri L.; Tan, Paula (2006). "Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment". J. Chem. Educ. 83 (11): 1654. Bibcode:2006JChEd..83.1654S. doi:10.1021/ed083p1654.

archive.org (Global: 6^th place; Galician: 4^th place)

Karakida, Ken-ichi; Fukuyama, Tsutomu; Kuchitsu, Kozo (1974). "Molecular Structures of Hydrogen Cyanide and Acetonitrile as Studied by Gas Electron Diffraction". Bulletin of the Chemical Society of Japan 47 (2): 299–304. doi:10.1246/bcsj.47.299.
Yamazaki, Shigekazu; Yamazaki, Yasuyuki (1990). "Nickel-catalyzed dehydrogenation of amines to nitriles". Bulletin of the Chemical Society of Japan 63 (1): 301–303. doi:10.1246/bcsj.63.301.
Chen, Fen-Er; Kuang, Yun-Yan; Hui-Fang, Dai; Lu, Liang (2003). "A Selective and Mild Oxidation of Primary Amines to Nitriles with Trichloroisocyanuric Acid". Synthesis 17 (17): 2629–2631. doi:10.1055/s-2003-42431.
Schäfer, H. J.; Feldhues, U. (1982). "Oxidation of Primary Aliphatic Amines to Nitriles at the Nickel Hydroxide Electrode". Synthesis 2 (2): 145–146. doi:10.1055/s-1982-29721.
Hiegel, Gene; Lewis, Justin; Bae, Jason (2004). "Conversion of α‐Amino Acids into Nitriles by Oxidative Decarboxylation with Trichloroisocyanuric Acid". Synthetic Communications 34 (19): 3449–3453. doi:10.1081/SCC-200030958.
Fleming, Fraser F.; Zhang, Zhiyu (24 de xaneiro de 2005). "Cyclic nitriles: tactical advantages in synthesis". Tetrahedron 61 (4): 747–789. doi:10.1016/j.tet.2004.11.012.
Smith, Andri L.; Tan, Paula (2006). "Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment". J. Chem. Educ. 83 (11): 1654. Bibcode:2006JChEd..83.1654S. doi:10.1021/ed083p1654.
Berkoff, Charles E.; Rivard, Donald E.; Kirkpatrick, David; Ives, Jeffrey L. (1980). "The Reductive Decyanation of Nitriles by Alkali Fusion". Synthetic Communications 10 (12): 939–945. doi:10.1080/00397918008061855.
Yoshiaki Nakao; Akira Yada; Shiro Ebata & Tamejiro Hiyama (2007). "A Dramatic Effect of Lewis-Acid Catalysts on Nickel-Catalyzed Carbocyanation of Alkynes" (Communication). J. Am. Chem. Soc. 129 (9): 2428–2429. PMID 17295484. doi:10.1021/ja067364x.
Rach, S. F.; Kühn, F. E. (2009). "Nitrile Ligated Transition Metal Complexes with Weakly Coordinating Counteranions and Their Catalytic Applications". Chemical Reviews 109 (5): 2061–2080. PMID 19326858. doi:10.1021/cr800270h.

books.google.com (Global: 3^rd place; Galician: 11^th place)

Gay-Lussac produciu cianuro de hidróxeno puro licuado en: Gay-Lussac (1811) "Note sur l'acide prussique" (Nota sobre o ácido prúsico), Annales de chimie, 44: 128 – 133.
J. Pelouze (1834). "Notiz über einen neuen Cyanäther" [Note on a new cyano-ether]. Annalen der Pharmacie 10 (3): 249. doi:10.1002/jlac.18340100302.
Hermann Fehling (1844). "Ueber die Zersetzung des benzoësauren Ammoniaks durch die Wärme (Sobre a descomposición do benzoato amónico pol calor)". Annalen der Chemie und Pharmacie 49 (1): 91–97. doi:10.1002/jlac.18440490106. Na páxina 96, Fehling escribiu: "Da Laurent den von ihm entdeckten Körper schon Nitrobenzoyl genannt hat, auch schon ein Azobenzoyl existirt, so könnte man den aus benzoësaurem Ammoniak entstehenden Körper vielleicht Benzonitril nennen." (Como Laurent nomeou a substancia que el descubrira "nitrobenzoíl" – tamén existía xa un "azobenzoíl" – talvez podemos chamar a substancia que se orixina a partir do benzoato de amonio "benzonitrilo".)

degruyter.com (Global: 927^th place; Galician: 872^nd place)

Abbas, Khamis A. (2008-01-01). "Substituent Effects on the Hydrolysis of p-Substituted Benzonitriles in Sulfuric Acid Solutions at (25.0± 0.1) °C". Zeitschrift für Naturforschung A 63 (9). ISSN 1865-7109. doi:10.1515/zna-2008-0912.

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

dx.doi.org

Karakida, Ken-ichi; Fukuyama, Tsutomu; Kuchitsu, Kozo (1974). "Molecular Structures of Hydrogen Cyanide and Acetonitrile as Studied by Gas Electron Diffraction". Bulletin of the Chemical Society of Japan 47 (2): 299–304. doi:10.1246/bcsj.47.299.
David T. Mowry (1948). "The Preparation of Nitriles" (– ^{Scholar search}). Chemical Reviews 42 (2): 189–283. PMID 18914000. doi:10.1021/cr60132a001.
J. Pelouze (1834). "Notiz über einen neuen Cyanäther" [Note on a new cyano-ether]. Annalen der Pharmacie 10 (3): 249. doi:10.1002/jlac.18340100302.
Hermann Fehling (1844). "Ueber die Zersetzung des benzoësauren Ammoniaks durch die Wärme (Sobre a descomposición do benzoato amónico pol calor)". Annalen der Chemie und Pharmacie 49 (1): 91–97. doi:10.1002/jlac.18440490106. Na páxina 96, Fehling escribiu: "Da Laurent den von ihm entdeckten Körper schon Nitrobenzoyl genannt hat, auch schon ein Azobenzoyl existirt, so könnte man den aus benzoësaurem Ammoniak entstehenden Körper vielleicht Benzonitril nennen." (Como Laurent nomeou a substancia que el descubrira "nitrobenzoíl" – tamén existía xa un "azobenzoíl" – talvez podemos chamar a substancia que se orixina a partir do benzoato de amonio "benzonitrilo".)
Peter Pollak, Gérard Romeder, Ferdinand Hagedorn, Heinz-Peter Gelbke "Nitriles" Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. doi 10.1002/14356007.a17_363
Gregory, Robert J. H. (1999). "Cyanohydrins in Nature and the Laboratory: Biology, Preparations, and Synthetic Applications". Chemical Reviews 99 (12): 3649–3682. PMID 11849033. doi:10.1021/cr9902906.
Chun-Wei Kuo; Jia-Liang Zhu; Jen-Dar Wu; Cheng-Ming Chu; Ching-Fa Yao; Kak-Shan Shia (2007). "A convenient new procedure for converting primary amides into nitriles". Chem. Commun. 2007 (3): 301–303. PMID 17299646. doi:10.1039/b614061k.
Reynold C. Fuson; Oscar R. Kreimeier & Gilbert L. Nimmo (1930). "Ring Closures in the Cyclobutane Series. II. Cyclization Of α,α′-Dibromo-Adipic Esters". J. Am. Chem. Soc. 52 (10): 4074–4076. doi:10.1021/ja01373a046.
A. P. N. Franchimont (1872). "Ueber die Dibenzyldicarbonsäure" [On 2,3-diphenylsuccinic acid]. Berichte der Deutschen Chemischen Gesellschaft 5 (2): 1048–1050. doi:10.1002/cber.187200502138.
J. Houben, Walter Fischer (1930) "Über eine neue Methode zur Darstellung cyclischer Nitrile durch katalytischen Abbau (I. Mitteil.)," Berichte der deutschen chemischen Gesellschaft (A and B Series) 63 (9): 2464 – 2472. doi 10.1002/cber.19300630920
Yamazaki, Shigekazu; Yamazaki, Yasuyuki (1990). "Nickel-catalyzed dehydrogenation of amines to nitriles". Bulletin of the Chemical Society of Japan 63 (1): 301–303. doi:10.1246/bcsj.63.301.
Chen, Fen-Er; Kuang, Yun-Yan; Hui-Fang, Dai; Lu, Liang (2003). "A Selective and Mild Oxidation of Primary Amines to Nitriles with Trichloroisocyanuric Acid". Synthesis 17 (17): 2629–2631. doi:10.1055/s-2003-42431.
Schäfer, H. J.; Feldhues, U. (1982). "Oxidation of Primary Aliphatic Amines to Nitriles at the Nickel Hydroxide Electrode". Synthesis 2 (2): 145–146. doi:10.1055/s-1982-29721.
Hiegel, Gene; Lewis, Justin; Bae, Jason (2004). "Conversion of α‐Amino Acids into Nitriles by Oxidative Decarboxylation with Trichloroisocyanuric Acid". Synthetic Communications 34 (19): 3449–3453. doi:10.1081/SCC-200030958.
Hampson, N; Lee, J; MacDonald, K (1972). "The oxidation of amino compounds at anodic silver". Electrochimica Acta 17 (5): 921–955. doi:10.1016/0013-4686(72)90014-X.
Dakin, Henry Drysdale (1916). "The Oxidation of Amino-Acids to Cyanides". Biochemical Journal 10 (2): 319–323. PMC 1258710. PMID 16742643. doi:10.1042/bj0100319.
Kukushkin, V. Yu.; Pombeiro, A. J. L. (2005). "Metal-mediated and metal-catalyzed hydrolysis of nitriles". Inorg. Chim. Acta 358: 1–21. doi:10.1016/j.ica.2004.04.029.
Abbas, Khamis A. (2008-01-01). "Substituent Effects on the Hydrolysis of p-Substituted Benzonitriles in Sulfuric Acid Solutions at (25.0± 0.1) °C". Zeitschrift für Naturforschung A 63 (9). ISSN 1865-7109. doi:10.1515/zna-2008-0912.
Barrault, J.; Pouilloux, Y. (1997). "Catalytic Amination Reactions: Synthesis of fatty amines. Selectivity control in presence of multifunctional catalysts". Catalysis Today 1997 (2): 137–153. doi:10.1016/S0920-5861(97)00006-0.
Fleming, Fraser F.; Zhang, Zhiyu (24 de xaneiro de 2005). "Cyclic nitriles: tactical advantages in synthesis". Tetrahedron 61 (4): 747–789. doi:10.1016/j.tet.2004.11.012.
Smith, Andri L.; Tan, Paula (2006). "Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment". J. Chem. Educ. 83 (11): 1654. Bibcode:2006JChEd..83.1654S. doi:10.1021/ed083p1654.
Mattalia, Jean-Marc; Marchi-Delapierre, Caroline; Hazimeh, Hassan & Chanon, Michel (2006-03-15). "The reductive decyanation reaction: chemical methods and synthetic applications". Arkivoc (en inglés) 2006 (4): 90. ISSN 1551-7012. doi:10.3998/ark.5550190.0007.408. AL-1755FR.
Berkoff, Charles E.; Rivard, Donald E.; Kirkpatrick, David; Ives, Jeffrey L. (1980). "The Reductive Decyanation of Nitriles by Alkali Fusion". Synthetic Communications 10 (12): 939–945. doi:10.1080/00397918008061855.
Yoshiaki Nakao; Akira Yada; Shiro Ebata & Tamejiro Hiyama (2007). "A Dramatic Effect of Lewis-Acid Catalysts on Nickel-Catalyzed Carbocyanation of Alkynes" (Communication). J. Am. Chem. Soc. 129 (9): 2428–2429. PMID 17295484. doi:10.1021/ja067364x.
Rach, S. F.; Kühn, F. E. (2009). "Nitrile Ligated Transition Metal Complexes with Weakly Coordinating Counteranions and Their Catalytic Applications". Chemical Reviews 109 (5): 2061–2080. PMID 19326858. doi:10.1021/cr800270h.
Fleming, Fraser F.; Yao, Lihua; Ravikumar, P. C.; Funk, Lee; Shook, Brian C. (novembro de 2010). "Nitrile-containing pharmaceuticals: efficacious roles of the nitrile pharmacophore". J Med Chem 53 (22): 7902–17. PMC 2988972. PMID 20804202. doi:10.1021/jm100762r.

google.co.uk (Global: 1,519^th place; Galician: 4,878^th place)

scholar.google.co.uk

David T. Mowry (1948). "The Preparation of Nitriles" (– ^{Scholar search}). Chemical Reviews 42 (2): 189–283. PMID 18914000. doi:10.1021/cr60132a001.

hathitrust.org (Global: 296^th place; Galician: 588^th place)

babel.hathitrust.org

A. P. N. Franchimont (1872). "Ueber die Dibenzyldicarbonsäure" [On 2,3-diphenylsuccinic acid]. Berichte der Deutschen Chemischen Gesellschaft 5 (2): 1048–1050. doi:10.1002/cber.187200502138.

hdl.handle.net (Global: 66^th place; Galician: 88^th place)

Mattalia, Jean-Marc; Marchi-Delapierre, Caroline; Hazimeh, Hassan & Chanon, Michel (2006-03-15). "The reductive decyanation reaction: chemical methods and synthetic applications". Arkivoc (en inglés) 2006 (4): 90. ISSN 1551-7012. doi:10.3998/ark.5550190.0007.408. AL-1755FR.

iupac.org (Global: 1,291^st place; Galician: 191^st place)

goldbook.iupac.org

IUPAC Gold Book nitriles

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

ncbi.nlm.nih.gov

NCBI-MeSH Nitriles
David T. Mowry (1948). "The Preparation of Nitriles" (– ^{Scholar search}). Chemical Reviews 42 (2): 189–283. PMID 18914000. doi:10.1021/cr60132a001.
Gregory, Robert J. H. (1999). "Cyanohydrins in Nature and the Laboratory: Biology, Preparations, and Synthetic Applications". Chemical Reviews 99 (12): 3649–3682. PMID 11849033. doi:10.1021/cr9902906.
Chun-Wei Kuo; Jia-Liang Zhu; Jen-Dar Wu; Cheng-Ming Chu; Ching-Fa Yao; Kak-Shan Shia (2007). "A convenient new procedure for converting primary amides into nitriles". Chem. Commun. 2007 (3): 301–303. PMID 17299646. doi:10.1039/b614061k.
Dakin, Henry Drysdale (1916). "The Oxidation of Amino-Acids to Cyanides". Biochemical Journal 10 (2): 319–323. PMC 1258710. PMID 16742643. doi:10.1042/bj0100319.
Yoshiaki Nakao; Akira Yada; Shiro Ebata & Tamejiro Hiyama (2007). "A Dramatic Effect of Lewis-Acid Catalysts on Nickel-Catalyzed Carbocyanation of Alkynes" (Communication). J. Am. Chem. Soc. 129 (9): 2428–2429. PMID 17295484. doi:10.1021/ja067364x.
Rach, S. F.; Kühn, F. E. (2009). "Nitrile Ligated Transition Metal Complexes with Weakly Coordinating Counteranions and Their Catalytic Applications". Chemical Reviews 109 (5): 2061–2080. PMID 19326858. doi:10.1021/cr800270h.
Fleming, Fraser F.; Yao, Lihua; Ravikumar, P. C.; Funk, Lee; Shook, Brian C. (novembro de 2010). "Nitrile-containing pharmaceuticals: efficacious roles of the nitrile pharmacophore". J Med Chem 53 (22): 7902–17. PMC 2988972. PMID 20804202. doi:10.1021/jm100762r.

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

W. Nagata and M. Yoshioka (1988). "Diethylaluminum cyanide". Org. Synth. cv6p0436.
W. Nagata, M. Yoshioka, and M. Murakami (1988). "Preparation of cyano compounds using alkylaluminum intermediates: 1-cyano-6-methoxy-3,4-dihydronaphthalene". Org. Synth. cv6p0307.

rsc.org (Global: 2,104^th place; Galician: 603^rd place)

pubs.rsc.org

Natural Product Reports Issue 5, 1999 Nitrile-containing natural products

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

Adams, Roger (1957). Organic Reactions, Volume 9. New York: John Wiley & Sons, Inc. ISBN 9780471007265. Arquivado dende o orixinal o 31 de outubro de 2014. Consultado o 18 July 2014.

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

Adams, Roger (1957). Organic Reactions, Volume 9. New York: John Wiley & Sons, Inc. ISBN 9780471007265. Arquivado dende o orixinal o 31 de outubro de 2014. Consultado o 18 July 2014.

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

Abbas, Khamis A. (2008-01-01). "Substituent Effects on the Hydrolysis of p-Substituted Benzonitriles in Sulfuric Acid Solutions at (25.0± 0.1) °C". Zeitschrift für Naturforschung A 63 (9). ISSN 1865-7109. doi:10.1515/zna-2008-0912.
Mattalia, Jean-Marc; Marchi-Delapierre, Caroline; Hazimeh, Hassan & Chanon, Michel (2006-03-15). "The reductive decyanation reaction: chemical methods and synthetic applications". Arkivoc (en inglés) 2006 (4): 90. ISSN 1551-7012. doi:10.3998/ark.5550190.0007.408. AL-1755FR.

Nitrilo (Galician Wikipedia)

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

pubs.acs.org

adsabs.harvard.edu (Global: 14th place; Galician: 17th place)

archive.org (Global: 6th place; Galician: 4th place)

books.google.com (Global: 3rd place; Galician: 11th place)

degruyter.com (Global: 927th place; Galician: 872nd place)

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

dx.doi.org

google.co.uk (Global: 1,519th place; Galician: 4,878th place)