酰胺 (Chinese Wikipedia)

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

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22doi.org

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4web.archive.org

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3archive.org

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3harvard.edu

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1ugent.be

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acdlabs.com

Organic Chemistry IUPAC Nomenclature. Rules C-821. Amides http://www.acdlabs.com/iupac/nomenclature/79/r79_540.htm 互联网档案馆的存檔，存档日期21 January 2011.

archive.org

Chapter 21: Amides and Imides. Nomenclature of Organic Compounds. Advances in Chemistry 126 (Washington, American Chemical Society). 1974: 166–173. ISBN 9780841201910. doi:10.1021/ba-1974-0126.ch021.
Valeur, Eric; Bradley, Mark. Amide bond formation: beyond the myth of coupling reagents. Chem. Soc. Rev. 2009, 38 (2): 606–631. PMID 19169468. S2CID 14950926. doi:10.1039/B701677H.
Chapman, Arthur William. CCLXIX.—Imino-aryl ethers. Part III. The molecular rearrangement of N-phenylbenziminophenyl ether. Journal of the Chemical Society, Transactions. 1925, 127: 1992–1998. doi:10.1039/CT9252701992.

books.google.com

Smith, Michael B.; March, Jerry, Advanced Organic Chemistry: Reactions, Mechanisms, and Structure 6th, New York: Wiley-Interscience, 2007, ISBN 978-0-471-72091-1

doi.org

國際純化學和應用化學聯合會，化學術語概略，第二版。（金皮書）(1997)。在線校正版: (2006–) "amides"。doi:10.1351/goldbook.A00266
Chapter 21: Amides and Imides. Nomenclature of Organic Compounds. Advances in Chemistry 126 (Washington, American Chemical Society). 1974: 166–173. ISBN 9780841201910. doi:10.1021/ba-1974-0126.ch021.
Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart. Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides (PDF). Journal of Ethnopharmacology. 2012, 142 (3): 563–590 [2022-07-12]. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714 . （原始内容 (PDF)存档于2022-07-14）.
Ivana Antol; Mirjana Eckert-Maksic; Hans Lischka. Ab Initio MR-CISD Study of Gas-Phase Basicity of Formamide in the First Excited Singlet State. The Journal of Physical Chemistry A. 2004, 108 (46): 10317–10325. doi:10.1021/jp048087o.
Yuko Otani; Osamu Nagae; Yuji Naruse; Satoshi Inagaki; Masashi Ohno; Kentaro Yamaguchi; Gaku Yamamoto; Masanobu Uchiyama; Tomohiko Ohwada. An Evaluation of Amide Group Planarity in 7-Azabicyclo[2.2.1]heptane Amides. Low Amide Bond Rotation Barrier in Solution. J. Am. Chem. Soc. 2003, 125 (49): 15191–15199. doi:10.1021/ja036644z.
Sayan Bagchi; Yung Sam Kim; Adam K. Charnley; Amos B. Smith; Robin M. Hochstrasser. Two-Dimensional Infrared Investigation of N-Acetyl Tryptophan Methyl Amide in Solution. The Journal of Physical Chemistry B. 2007, 111 (11): 3010–3018. doi:10.1021/jp067348m.
A. R. Goldfarb; A. Mele; N. Gutstein. Basicity of the Amide Bond. J. Am. Chem. Soc. 1955, 77 (23): 6194–6196. doi:10.1021/ja01628a031.
Yang Han; Tao Hou; Zi-Hui Zhang; Yao-Dong Wang; Jun-Xiang Cheng; Han Zhou; Ji-Xia Wang; Jia-Tao Feng; Yan-Fang Liu; Zhi-Mou Guo; Xin-Miao Liang. Structurally diverse isoquinoline and amide alkaloids with dopamine D2 receptor antagonism from Corydalis bungeana. Fitoterapia. 2022, 159: 105175. ISSN 0367-326X. doi:10.1016/j.fitote.2022.105175.
Montalbetti, Christian A. G. N.; Falque, Virginie. Amide bond formation and peptide coupling. Tetrahedron. 14 November 2005, 61 (46): 10827–10852. doi:10.1016/j.tet.2005.08.031.
Valeur, Eric; Bradley, Mark. Amide bond formation: beyond the myth of coupling reagents. Chem. Soc. Rev. 2009, 38 (2): 606–631. PMID 19169468. S2CID 14950926. doi:10.1039/B701677H.
Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. Borate esters: Simple catalysts for the sustainable synthesis of complex amides. Science Advances. 2017-09-01, 3 (9): e1701028. Bibcode:2017SciA....3E1028S. PMC 5609808 . PMID 28948222. doi:10.1126/sciadv.1701028.
Wenner, Wilhelm. Phenylacetamide. Organic Syntheses. 1952, 32: 92. doi:10.15227/orgsyn.032.0092.
Karl Kindler. Studien über den Mechanismus chemischer Reaktionen. Erste Abhandlung. Reduktion von Amiden und Oxydation von Aminen. Liebigs Annalen. 1923, 431 (1): 187–230. doi:10.1002/jlac.19234310111.
Schulenberg, J. W.; Archer, S. The Chapman Rearrangement 14. 1965: 1–51. ISBN 978-0471264187. doi:10.1002/0471264180.or014.01.
Chapman, Arthur William. CCLXIX.—Imino-aryl ethers. Part III. The molecular rearrangement of N-phenylbenziminophenyl ether. Journal of the Chemical Society, Transactions. 1925, 127: 1992–1998. doi:10.1039/CT9252701992.
Adams, Rodger; Krimen, L.I.; Cota, Donald J. Organic Reaction Volume 17. London: John Wiley & Sons, Inc. 1969: 213–326. ISBN 9780471196150. doi:10.1002/0471264180.
Corson, B. B.; Scott, R. W.; Vose, C. E. Cyanoacetamide. Organic Syntheses. 1941, 1: 179. doi:10.15227/orgsyn.009.0036.
Jacobs, W. A. Chloroacetamide. Organic Syntheses. 1941, 1: 153. doi:10.15227/orgsyn.007.0016.
Kleinberg, J.; Audrieth, L. F. Lactamide. Organic Syntheses. 1955, 3: 516. doi:10.15227/orgsyn.021.0071.
Gunanathan, C.; Ben-David, Y.; Milstein, D. Direct Synthesis of Amides from Alcohols and Amines with Liberation of H₂. Science. 2007, 317 (5839): 790–2. Bibcode:2007Sci...317..790G. PMID 17690291. S2CID 43671648. doi:10.1126/science.1145295.
T. A. Dineen; M. A. Zajac; A. G. Myers. Efficient Transamidation of Primary Carboxamides by in situ Activation with N,N-Dialkylformamide Dimethyl Acetals. J. Am. Chem. Soc. 2006, 128 (50): 16406–16409. PMID 17165798. doi:10.1021/ja066728i.
Emma L. Baker; Michael M. Yamano; Yujing Zhou; Sarah M. Anthony; Neil K. Garg. A two-step approach to achieve secondary amide transamidation enabled by nickel catalysis. Nature Communications. 2016, 7: 11554. Bibcode:2016NatCo...711554B. PMC 4876455 . PMID 27199089. doi:10.1038/ncomms11554.

google.com

美國專利第5,935,953号

handle.net

hdl.handle.net

Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart. Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides (PDF). Journal of Ethnopharmacology. 2012, 142 (3): 563–590 [2022-07-12]. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714 . （原始内容 (PDF)存档于2022-07-14）.

harvard.edu

ui.adsabs.harvard.edu

Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. Borate esters: Simple catalysts for the sustainable synthesis of complex amides. Science Advances. 2017-09-01, 3 (9): e1701028. Bibcode:2017SciA....3E1028S. PMC 5609808 . PMID 28948222. doi:10.1126/sciadv.1701028.
Gunanathan, C.; Ben-David, Y.; Milstein, D. Direct Synthesis of Amides from Alcohols and Amines with Liberation of H₂. Science. 2007, 317 (5839): 790–2. Bibcode:2007Sci...317..790G. PMID 17690291. S2CID 43671648. doi:10.1126/science.1145295.
Emma L. Baker; Michael M. Yamano; Yujing Zhou; Sarah M. Anthony; Neil K. Garg. A two-step approach to achieve secondary amide transamidation enabled by nickel catalysis. Nature Communications. 2016, 7: 11554. Bibcode:2016NatCo...711554B. PMC 4876455 . PMID 27199089. doi:10.1038/ncomms11554.

iupac.org

goldbook.iupac.org

國際純化學和應用化學聯合會，化學術語概略，第二版。（金皮書）(1997)。在線校正版: (2006–) "amides"。doi:10.1351/goldbook.A00266

nih.gov

ncbi.nlm.nih.gov

Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart. Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides (PDF). Journal of Ethnopharmacology. 2012, 142 (3): 563–590 [2022-07-12]. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714 . （原始内容 (PDF)存档于2022-07-14）.
Valeur, Eric; Bradley, Mark. Amide bond formation: beyond the myth of coupling reagents. Chem. Soc. Rev. 2009, 38 (2): 606–631. PMID 19169468. S2CID 14950926. doi:10.1039/B701677H.
Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. Borate esters: Simple catalysts for the sustainable synthesis of complex amides. Science Advances. 2017-09-01, 3 (9): e1701028. Bibcode:2017SciA....3E1028S. PMC 5609808 . PMID 28948222. doi:10.1126/sciadv.1701028.
Gunanathan, C.; Ben-David, Y.; Milstein, D. Direct Synthesis of Amides from Alcohols and Amines with Liberation of H₂. Science. 2007, 317 (5839): 790–2. Bibcode:2007Sci...317..790G. PMID 17690291. S2CID 43671648. doi:10.1126/science.1145295.
T. A. Dineen; M. A. Zajac; A. G. Myers. Efficient Transamidation of Primary Carboxamides by in situ Activation with N,N-Dialkylformamide Dimethyl Acetals. J. Am. Chem. Soc. 2006, 128 (50): 16406–16409. PMID 17165798. doi:10.1021/ja066728i.
Emma L. Baker; Michael M. Yamano; Yujing Zhou; Sarah M. Anthony; Neil K. Garg. A two-step approach to achieve secondary amide transamidation enabled by nickel catalysis. Nature Communications. 2016, 7: 11554. Bibcode:2016NatCo...711554B. PMC 4876455 . PMID 27199089. doi:10.1038/ncomms11554.

nootropicsfrontline.com

Monson, Richard. Advanced Organic Synthesis: Methods and Techniques (PDF). New York: Academic Press. 1971: 141 [2022-07-26]. ISBN 978-0124336803. （原始内容 (PDF)存档于2021-11-04）.

semanticscholar.org

api.semanticscholar.org

Valeur, Eric; Bradley, Mark. Amide bond formation: beyond the myth of coupling reagents. Chem. Soc. Rev. 2009, 38 (2): 606–631. PMID 19169468. S2CID 14950926. doi:10.1039/B701677H.
Gunanathan, C.; Ben-David, Y.; Milstein, D. Direct Synthesis of Amides from Alcohols and Amines with Liberation of H₂. Science. 2007, 317 (5839): 790–2. Bibcode:2007Sci...317..790G. PMID 17690291. S2CID 43671648. doi:10.1126/science.1145295.

sigmaaldrich.com

Tris(2,2,2-trifluoroethyl) borate 97% | Sigma-Aldrich. www.sigmaaldrich.com. [2016-09-22].

ugent.be

biblio.ugent.be

Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart. Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides (PDF). Journal of Ethnopharmacology. 2012, 142 (3): 563–590 [2022-07-12]. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714 . （原始内容 (PDF)存档于2022-07-14）.

ukim.edu.mk

pmf.ukim.edu.mk

Bodroux reaction. Institute of Chemistry, Skopje, Macedonia. [23 May 2007]. （原始内容存档于24 September 2015）.

web.archive.org

Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart. Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides (PDF). Journal of Ethnopharmacology. 2012, 142 (3): 563–590 [2022-07-12]. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714 . （原始内容 (PDF)存档于2022-07-14）.
Organic Chemistry IUPAC Nomenclature. Rules C-821. Amides http://www.acdlabs.com/iupac/nomenclature/79/r79_540.htm 互联网档案馆的存檔，存档日期21 January 2011.
Bodroux reaction. Institute of Chemistry, Skopje, Macedonia. [23 May 2007]. （原始内容存档于24 September 2015）.
Monson, Richard. Advanced Organic Synthesis: Methods and Techniques (PDF). New York: Academic Press. 1971: 141 [2022-07-26]. ISBN 978-0124336803. （原始内容 (PDF)存档于2021-11-04）.

worldcat.org

Yang Han; Tao Hou; Zi-Hui Zhang; Yao-Dong Wang; Jun-Xiang Cheng; Han Zhou; Ji-Xia Wang; Jia-Tao Feng; Yan-Fang Liu; Zhi-Mou Guo; Xin-Miao Liang. Structurally diverse isoquinoline and amide alkaloids with dopamine D2 receptor antagonism from Corydalis bungeana. Fitoterapia. 2022, 159: 105175. ISSN 0367-326X. doi:10.1016/j.fitote.2022.105175.