Benzylamine (Vietnamese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Benzylamine" in Vietnamese language version.

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14doi.org

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8nih.gov

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books.google.com

Schomburg, D.; Schomburg, I.; Chang, A. biên tập (2009). “3.5.1.91 N-substituted formamide deformylase”. Class 3 Hydrolases: EC 3.4.22–3.13. Springer Handbook of Enzymes (ấn bản thứ 2). Springer Science & Business Media. tr. 376–378. ISBN 9783540857051.
Li, J. J. (2014). “Schotten–Baumann reaction”. Name Reactions: A Collection of Detailed Mechanisms and Synthetic Applications (ấn bản thứ 5). Springer. tr. 362. ISBN 9783319039794.
Anderson, N. G. (2012). “5. Solvent Selection”. Practical Process Research and Development – A guide for Organic Chemists (ấn bản thứ 2). Academic Press. tr. 121–168. ISBN 9780123865380.
Odian, G. (2004). “2.8c – Interfacial Polymerization”. Principles of Polymerization (ấn bản thứ 4). John Wiley & Sons. tr. 90–92. ISBN 9780471274001.
Li, J. J. (2014). “Schlittler–Müller modification”. Name Reactions: A Collection of Detailed Mechanisms and Synthetic Applications (ấn bản thứ 5). Springer. tr. 492. ISBN 9783319039794.
Peterson, U. (2006). “Quinolone Antibiotics: The Development of Moxifloxacin”. Trong IUPAC; Fischer, J.; Ganellin, C. R. (biên tập). Analogue-based Drug Discovery. John Wiley & Sons. tr. 338–342. ISBN 9783527607495.
Hellgren, U.; Ericsson, Ö.; Aden Abdi, Y.; Gustafsson, L. L. (2003). “Bephenium hydroxynaphthoate”. Handbook of Drugs for Tropical Parasitic Infections (ấn bản thứ 2). CRC Press. tr. 33–35. ISBN 9780203211519.

doi.org

Hall, H. K. (1957). "Correlation of the Base Strengths of Amines". J. Am. Chem. Soc. 79 (20): 5441–5444. doi:10.1021/ja01577a030.
Heuer, L. (2006). “Benzylamines”. Ullmann's Encyclopedia of Industrial Chemistry. Wiley-VCH. doi:10.1002/14356007.a04_009.pub2. ISBN 3527306730.
Crossley, F. S.; Moore, M. L. (1944). “Studies on the Leuckart Reaction”. J. Org. Chem. 9 (6): 529–536. doi:10.1021/jo01188a006.
Webers, V. J.; Bruce, W. F. (1948). “The Leuckart Reaction: A study of the Mechanism”. J. Am. Chem. Soc. 70 (4): 1422–1424. doi:10.1021/ja01184a038.
Pollard, C. B.; Young, D. C. (1951). “The Mechanism of the Leuckart Reaction”. J. Org. Chem. 16 (5): 661–672. doi:10.1021/jo01145a001.
Fukatsu, H.; Hashimoto, Y.; Goda, M.; Higashibata, H.; Kobayashi, M. (2004). “Amine-synthesizing enzyme N-substituted formamide deformylase: screening, purification, characterization, and gene cloning”. Proc. Natl. Acad. Sci. 101 (38): 13726–13731. doi:10.1073/pnas.0405082101. PMC 518824. PMID 15358859.
Tipton, K. F.; Boyce, S.; O'Sullivan, J.; Davey, G. P.; Healy, J. (2004). “Monoamine oxidases: Certainties and uncertainties”. Curr. Med. Chem. 11 (15): 1965–1982. doi:10.2174/0929867043364810. PMID 15279561.
Schotten, C. (1884). “Ueber die Oxydation des Piperidins”. Ber. Dtsch. Chem. Ges. (bằng tiếng Đức). 17 (2): 2544–2547. doi:10.1002/cber.188401702178.
Baumann, E. (1886). “Ueber eine einfache Methode der Darstellung von Benzoësäureäthern”. Ber. Dtsch. Chem. Ges. 19 (2): 3218–3222. doi:10.1002/cber.188601902348.
Grieco, P. A.; Larsen, S. D. (1990). “N-benzyl-2-azanorbornene”. Organic Syntheses. 68: 206. doi:10.15227/orgsyn.068.0206.
Lommen, G.; De Bruyn, M.; Schroven, M.; Verschueren, W.; Janssens, W.; Verrelst, J.; Leysen, J. (1995). “The discovery of a series of new non-indole 5HT_1D agonists”. Bioorg. Med. Chem. Lett. 5 (22): 2649–2654. doi:10.1016/0960-894X(95)00473-7.
Choi, D.; Stables, J. P.; Kohn, H. (1996). “Synthesis and anticonvulsant activities of N-Benzyl-2-acetamidopropionamide derivatives”. J. Med. Chem. 39 (9): 1907–1916. doi:10.1021/jm9508705. PMID 8627614.
Morieux, P.; Stables, J. P.; Kohn, H. (2008). “Synthesis and anticonvulsant activities of N-benzyl-(2R)-2-acetamido-3-oxysubstituted propionamide derivatives”. Bioorg. Med. Chem. 16 (19): 8968–8975. doi:10.1016/j.bmc.2008.08.055. PMC 2701728. PMID 18789868.
Nair, U. R.; Sivabalan, R.; Gore, G. M.; Geetha, M.; Asthana, S. N.; Singh, H. (2005). “Hexanitrohexaazaisowurtzitane (CL-20) and CL-20-based formulations (review)”. Combust. Explos. Shock Waves. 41 (2): 121–132. doi:10.1007/s10573-005-0014-2.

espacenet.com

v3.espacenet.com

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Đăng ký phát minh {{{country}}} {{{number}}}, "Benzylamine derivatives", trao vào [[{{{gdate}}}]] . Full text

google.com

Đăng ký phát minh {{{country}}} {{{number}}}, "{{{title}}}", trao vào [[{{{gdate}}}]] . Full text
Đăng ký phát minh {{{country}}} {{{number}}}, "Benzylamine derivatives", trao vào [[{{{gdate}}}]] . Full text

itrust.de

gestis-en.itrust.de

Record^{[liên kết hỏng]} in the GESTIS Substance Database of the Institute for Occupational Safety and Health

nasa.gov

history.nasa.gov

Swenson, L. S.; Grimwood, J. M.; Alexander, C. C. “13: Mercury Mission Accomplished (13.1 Preparing a Man to Orbit)”. This New Ocean: A History of Project Mercury. nasa.gov. tr. 413–418.

nih.gov

pubmed.ncbi.nlm.nih.gov

Fukatsu, H.; Hashimoto, Y.; Goda, M.; Higashibata, H.; Kobayashi, M. (2004). “Amine-synthesizing enzyme N-substituted formamide deformylase: screening, purification, characterization, and gene cloning”. Proc. Natl. Acad. Sci. 101 (38): 13726–13731. doi:10.1073/pnas.0405082101. PMC 518824. PMID 15358859.
Tipton, K. F.; Boyce, S.; O'Sullivan, J.; Davey, G. P.; Healy, J. (2004). “Monoamine oxidases: Certainties and uncertainties”. Curr. Med. Chem. 11 (15): 1965–1982. doi:10.2174/0929867043364810. PMID 15279561.
Choi, D.; Stables, J. P.; Kohn, H. (1996). “Synthesis and anticonvulsant activities of N-Benzyl-2-acetamidopropionamide derivatives”. J. Med. Chem. 39 (9): 1907–1916. doi:10.1021/jm9508705. PMID 8627614.
Morieux, P.; Stables, J. P.; Kohn, H. (2008). “Synthesis and anticonvulsant activities of N-benzyl-(2R)-2-acetamido-3-oxysubstituted propionamide derivatives”. Bioorg. Med. Chem. 16 (19): 8968–8975. doi:10.1016/j.bmc.2008.08.055. PMC 2701728. PMID 18789868.

ncbi.nlm.nih.gov

Fukatsu, H.; Hashimoto, Y.; Goda, M.; Higashibata, H.; Kobayashi, M. (2004). “Amine-synthesizing enzyme N-substituted formamide deformylase: screening, purification, characterization, and gene cloning”. Proc. Natl. Acad. Sci. 101 (38): 13726–13731. doi:10.1073/pnas.0405082101. PMC 518824. PMID 15358859.
“MAOB: Monoamine oxidase B – Homo sapiens”. National Center for Biotechnology Information. ngày 6 tháng 12 năm 2015. Truy cập ngày 29 tháng 12 năm 2015.
Morieux, P.; Stables, J. P.; Kohn, H. (2008). “Synthesis and anticonvulsant activities of N-benzyl-(2R)-2-acetamido-3-oxysubstituted propionamide derivatives”. Bioorg. Med. Chem. 16 (19): 8968–8975. doi:10.1016/j.bmc.2008.08.055. PMC 2701728. PMID 18789868.

pubchem.ncbi.nlm.nih.gov

PubChem Public Chemical Database (ngày 26 tháng 12 năm 2015). “1-Phenylethylamine”. National Center for Biotechnology Information. Truy cập ngày 29 tháng 12 năm 2015.

orgsyn.org

Gatto, V. J.; Miller, S. R.; Gokel, G. W. (1993). “4,13-Diaza-18-Crown-6”. Organic Syntheses.; Collective Volume, 8, tr. 152 (example of alklylation of benzylamine followed by hydrogenolysis).
Grieco, P. A.; Larsen, S. D. (1990). “N-benzyl-2-azanorbornene”. Organic Syntheses. 68: 206. doi:10.15227/orgsyn.068.0206.

phys.org

Yirka, B. (ngày 9 tháng 9 năm 2011). “University chemists devise means to stabilize explosive CL-20”. Phys.org. Truy cập ngày 28 tháng 12 năm 2015.

sigmaaldrich.com

"Benzylamine". Sigma-Aldrich. Truy cập 28 December 2015.
“Benzylamine hydrochloride”. Sigma-Aldrich. Truy cập ngày 28 tháng 12 năm 2015.

zenodo.org

Baumann, E. (1886). “Ueber eine einfache Methode der Darstellung von Benzoësäureäthern”. Ber. Dtsch. Chem. Ges. 19 (2): 3218–3222. doi:10.1002/cber.188601902348.