腈 (Chinese Wikipedia)

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

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10doi.org

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2orgsyn.org

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2drugfuture.com

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1iupac.org

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1wisc.edu

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acs.org

pubs.acs.org

David T. Mowry. The Preparation of Nitriles (^{[失效連結]} – ^{Scholar search}). Chemical Reviews. 1948, 42 (2): 189–283. doi:10.1021/cr60132a001. ^{[永久失效連結]}

archive-it.org

wayback.archive-it.org

Sharwan K, Dewan, Ravinder Singh, and Anil Kumar. One pot synthesis of nitriles from aldehydes and hydroxylamine hydrochloride using sodium sulfate (anhyd) and sodium bicarbonate in dry media under microwave irradiation (PDF). Arkivoc. 2006: (ii) 41–44 [2011-03-06]. （原始内容 (open access)存档于2007-09-26）.

arkat-usa.org

Sharwan K, Dewan, Ravinder Singh, and Anil Kumar. One pot synthesis of nitriles from aldehydes and hydroxylamine hydrochloride using sodium sulfate (anhyd) and sodium bicarbonate in dry media under microwave irradiation (PDF). Arkivoc. 2006: (ii) 41–44 [2011-03-06]. （原始内容 (open access)存档于2007-09-26）.
The reductive decyanation reaction: chemical methods and synthetic applications Jean-Marc Mattalia, Caroline Marchi-Delapierre, Hassan Hazimeh, and Michel Chanon Arkivoc (AL-1755FR) pp 90-118 2006 Article^{[永久失效連結]}

doi.org

David T. Mowry. The Preparation of Nitriles (^{[失效連結]} – ^{Scholar search}). Chemical Reviews. 1948, 42 (2): 189–283. doi:10.1021/cr60132a001. ^{[永久失效連結]}
J. Pelouze. Notiz über einen neuen Cyanäther. Annalen der Chemie und Pharmacie. 1834, 10 (2): 249. doi:10.1002/jlac.18340100302.
Hermann Fehling. Ueber die Zersetzung des benzoësauren Ammoniaks durch die Wärme. Annalen der Chemie und Pharmacie. 1844, 49 (1): 91–97. doi:10.1002/jlac.18440490106.
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
Chun-Wei Kuo, Jia-Liang Zhu, Jen-Dar Wu, Cheng-Ming Chu, Ching-Fa Yao and Kak-Shan Shia. A convenient new procedure for converting primary amides into nitriles. Chem. Commun. 2007, 2007 (3): 301–303. PMID 17299646. doi:10.1039/b614061k.
Reynold C. Fuson, Oscar R. Kreimeier, and Gilbert L. Nimmo. Ring Closures In The Cyclobutane Series. Ii. Cyclization Of Α,Α′-Dibromo-Adipic Esters. J. Am. Chem. Soc. 1930, 52 (10): 4074–4076. doi:10.1021/ja01373a046.
Über eine neue Methode zur Darstellung cyclischer Nitrile durch katalytischen Abbau (I. Mitteil.) (p 2464-2472) J. Houben, Walter Fischer Berichte der deutschen chemischen Gesellschaft (A and B Series) Volume 63, Issue 9 , Pages 2464 - 2472 doi:10.1002/cber.19300630920
Smith, Andri L.; Tan, Paula. Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment. J. Chem. Educ. 2006, 83: 1654 [2011-03-06]. doi:10.1021/ed083p1654. （原始内容存档于2008-07-04）.
Yoshiaki Nakao, Akira Yada, Shiro Ebata, and Tamejiro Hiyama. A Dramatic Effect of Lewis-Acid Catalysts on Nickel-Catalyzed Carbocyanation of Alkynes. J. Am. Chem. Soc. (Communication). 2007, 129 (9): 2428–2429. PMID 17295484. doi:10.1021/ja067364x.

dx.doi.org

Tetrahedron Volume 61, Issue 4, 24 January 2005, Pages 747-789 doi:10.1016/j.tet.2004.11.012

drugfuture.com

Franchimont Reaction. [2011-03-06]. （原始内容存档于2020-09-28）.
http://www.drugfuture.com/OrganicNameReactions/ONR197.htm （页面存档备份，存于互联网档案馆） Merck & Co., Inc., Whitehouse Station

google.co.uk

scholar.google.co.uk

David T. Mowry. The Preparation of Nitriles (^{[失效連結]} – ^{Scholar search}). Chemical Reviews. 1948, 42 (2): 189–283. doi:10.1021/cr60132a001. ^{[永久失效連結]}

ibucm.com

class.ibucm.com

羧酸的制备——腈水解（页面存档备份，存于互联网档案馆）. 北京中医药大学远程教育学院

iupac.org

goldbook.iupac.org

IUPAC Gold Book nitriles （页面存档备份，存于互联网档案馆）

nih.gov

ncbi.nlm.nih.gov

NCBI-MeSH Nitriles （页面存档备份，存于互联网档案馆）
Chun-Wei Kuo, Jia-Liang Zhu, Jen-Dar Wu, Cheng-Ming Chu, Ching-Fa Yao and Kak-Shan Shia. A convenient new procedure for converting primary amides into nitriles. Chem. Commun. 2007, 2007 (3): 301–303. PMID 17299646. doi:10.1039/b614061k.
Yoshiaki Nakao, Akira Yada, Shiro Ebata, and Tamejiro Hiyama. A Dramatic Effect of Lewis-Acid Catalysts on Nickel-Catalyzed Carbocyanation of Alkynes. J. Am. Chem. Soc. (Communication). 2007, 129 (9): 2428–2429. PMID 17295484. doi:10.1021/ja067364x.

orgsyn.org

W. Nagata and M. Yoshioka (1988). "Diethylaluminum cyanide". Org. Synth.; Coll. Vol. 6: 436.
W. Nagata, M. Yoshioka, and M. Murakami (1988). "PREPARATION OF CYANO COMPOUNDS USING ALKYLALUMINUM INTERMEDIATES: 1-CYANO-6-METHOXY-3,4-DIHYDRONAPHTHALENE". Org. Synth.; Coll. Vol. 6: 307.

web.archive.org

IUPAC Gold Book nitriles （页面存档备份，存于互联网档案馆）
NCBI-MeSH Nitriles （页面存档备份，存于互联网档案馆）
Franchimont Reaction. [2011-03-06]. （原始内容存档于2020-09-28）.
http://www.drugfuture.com/OrganicNameReactions/ONR197.htm （页面存档备份，存于互联网档案馆） Merck & Co., Inc., Whitehouse Station
羧酸的制备——腈水解（页面存档备份，存于互联网档案馆）. 北京中医药大学远程教育学院
Smith, Andri L.; Tan, Paula. Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment. J. Chem. Educ. 2006, 83: 1654 [2011-03-06]. doi:10.1021/ed083p1654. （原始内容存档于2008-07-04）.

wisc.edu

jchemed.chem.wisc.edu

Smith, Andri L.; Tan, Paula. Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment. J. Chem. Educ. 2006, 83: 1654 [2011-03-06]. doi:10.1021/ed083p1654. （原始内容存档于2008-07-04）.