Nitril (Romanian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Nitril" in Romanian language version.
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acs.org
pubs.acs.org
- en David T. Mowry (). „The Preparation of Nitriles” (– Scholar search). Chemical Reviews. 42 (2): 189–283. doi:10.1021/cr60132a001. PMID 18914000. [nefuncțională]
arkat-usa.org
- en 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” (open access). Arkivoc: (ii) 41–44.
- en 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
books.google.com
- en Gay-Lussac produced pure, liquified hydrogen cyanide in: Gay-Lussac (1811) "Note sur l'acide prussique" (Note on prussic acid), Annales de chimie, 44: 128 – 133.
- en J. Pelouze (). „Notiz über einen neuen Cyanäther” [Note on a new cyano-ether]. Annalen der Pharmacie. 10 (3): 249. doi:10.1002/jlac.18340100302.
- en Hermann Fehling (). „Ueber die Zersetzung des benzoësauren Ammoniaks durch die Wärme (On the decomposition of ammonium benzoate by heat)”. Annalen der Chemie und Pharmacie. 49 (1): 91–97. doi:10.1002/jlac.18440490106. On page 96, Fehling writes: "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." (Since Laurent named the substance that was discovered by him "nitrobenzoyl" – also an "azobenzoyl" already exists – so one could name the substance that originates from ammonium benzoate perhaps "benzonitril".)
doi.org
doi.org
- en David T. Mowry (). „The Preparation of Nitriles” (– Scholar search). Chemical Reviews. 42 (2): 189–283. doi:10.1021/cr60132a001. PMID 18914000. [nefuncțională]
- en J. Pelouze (). „Notiz über einen neuen Cyanäther” [Note on a new cyano-ether]. Annalen der Pharmacie. 10 (3): 249. doi:10.1002/jlac.18340100302.
- en Hermann Fehling (). „Ueber die Zersetzung des benzoësauren Ammoniaks durch die Wärme (On the decomposition of ammonium benzoate by heat)”. Annalen der Chemie und Pharmacie. 49 (1): 91–97. doi:10.1002/jlac.18440490106. On page 96, Fehling writes: "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." (Since Laurent named the substance that was discovered by him "nitrobenzoyl" – also an "azobenzoyl" already exists – so one could name the substance that originates from ammonium benzoate perhaps "benzonitril".)
- en 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 (3): 301–303. doi:10.1039/b614061k. PMID 17299646.
- en 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. 52 (10): 4074–4076. doi:10.1021/ja01373a046.
- en Yamazaki, Shigekazu; Yamazaki, Yasuyuki (). „Nickel-catalyzed dehydrogenation of amines to nitriles”. Bulletin of the Chemical Society of Japan. 63 (1): 301–303. doi:10.1246/bcsj.63.301.
- en Chen, Fen-Er; Kuang, Yun-Yan; Hui-Fang, Dai; Lu, Liang (). „A Selective and Mild Oxidation of Primary Amines to Nitriles with Trichloroisocyanuric Acid”. Synthesis. 17: 2629–2631. doi:10.1055/s-2003-42431.
- en Schäfer, H. J.; Feldhues, U. (). „Oxidation of Primary Aliphatic Amines to Nitriles at the Nickel Hydroxide Electrode”. 2: 145–146. doi:10.1055/s-1982-29721.
- en Hiegel, Gene; Lewis, Justin; Bae, Jason (). „Conversion of α‐Amino Acids into Nitriles by Oxidative Decarboxylation with Trichloroisocyanuric Acid”. Synthetic Communications. 34 (19): 3449–3453. doi:10.1081/SCC-200030958.
- en Hampson, N; Lee, J; MacDonald, K (). „The oxidation of amino compounds at anodic silver”. Electrochimica Acta. 17 (5): 921–955. doi:10.1016/0013-4686(72)90014-X.
- en Smith, Andri L.; Tan, Paula (). „Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment”. J. Chem. Educ. 83 (11): 1654. Bibcode:2006JChEd..83.1654S. doi:10.1021/ed083p1654. Arhivat din original la . Accesat în .
- en Fleming, Fraser F.; Yao, Lihua; Ravikumar, P. C.; Funk, Lee; Shook, Brian C. (noiembrie 2010). „Nitrile-containing pharmaceuticals: efficacious roles of the nitrile pharmacophore”. J Med Chem. 53 (22): 7902–17. doi:10.1021/jm100762r. PMC 2988972
. PMID 20804202.
dx.doi.org
- en 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
- en 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
- en Tetrahedron Volume 61, Issue 4, 24 January 2005, Pages 747–789 doi:10.1016/j.tet.2004.11.012
drugfuture.com
- en Franchimont Reaction
- en http://www.drugfuture.com/OrganicNameReactions/ONR197.htm Merck & Co., Inc., Whitehouse Station
google.co.uk
scholar.google.co.uk
- en David T. Mowry (). „The Preparation of Nitriles” (– Scholar search). Chemical Reviews. 42 (2): 189–283. doi:10.1021/cr60132a001. PMID 18914000. [nefuncțională]
harvard.edu
adsabs.harvard.edu
- en Smith, Andri L.; Tan, Paula (). „Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment”. J. Chem. Educ. 83 (11): 1654. Bibcode:2006JChEd..83.1654S. doi:10.1021/ed083p1654. Arhivat din original la . Accesat în .
nih.gov
ncbi.nlm.nih.gov
- en NCBI-MeSH Nitriles
- en David T. Mowry (). „The Preparation of Nitriles” (– Scholar search). Chemical Reviews. 42 (2): 189–283. doi:10.1021/cr60132a001. PMID 18914000. [nefuncțională]
- en 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 (3): 301–303. doi:10.1039/b614061k. PMID 17299646.
- en Dakin, Henry Drysdale (). „The Oxidation of Amino-Acids to Cyanides”. Biochemical Journal. 10 (2): 319–323. PMC 1258710 .
- en Fleming, Fraser F.; Yao, Lihua; Ravikumar, P. C.; Funk, Lee; Shook, Brian C. (noiembrie 2010). „Nitrile-containing pharmaceuticals: efficacious roles of the nitrile pharmacophore”. J Med Chem. 53 (22): 7902–17. doi:10.1021/jm100762r. PMC 2988972 . PMID 20804202.
orgsyn.org
- en W. Nagata and M. Yoshioka (), „Diethylaluminum cyanide”, Org. Synth.; Collective Volume, 6, p. 436
- en W. Nagata, M. Yoshioka, and M. Murakami (), „Preparation of cyano compounds using alkylaluminum intermediates: 1-cyano-6-methoxy-3,4-dihydronaphthalene”, Org. Synth.; Collective Volume, 6, p. 307
unibuc.ro
web.archive.org
- en Smith, Andri L.; Tan, Paula (). „Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment”. J. Chem. Educ. 83 (11): 1654. Bibcode:2006JChEd..83.1654S. doi:10.1021/ed083p1654. Arhivat din original la . Accesat în .
wiley.com
- en Adams, Roger (). Organic Reactions, Volume 9. New York: John Wiley & Sons, Inc. ISBN 9780471007265. Accesat în .
wisc.edu
jchemed.chem.wisc.edu
- en Smith, Andri L.; Tan, Paula (). „Creatine Synthesis: An Undergraduate Organic Chemistry Laboratory Experiment”. J. Chem. Educ. 83 (11): 1654. Bibcode:2006JChEd..83.1654S. doi:10.1021/ed083p1654. Arhivat din original la . Accesat în .