아마이드 (Korean Wikipedia)

Analysis of information sources in references of the Wikipedia article "아마이드" in Korean language version.

refsWebsite

Global rank Korean rank

19doi.org

2^nd place

3^rd place

8nih.gov

4^th place

5archive.org

6^th place

18^th place

3harvard.edu

18^th place

27^th place

2web.archive.org

1^st place

2ghostarchive.org

32^nd place

656^th place

2semanticscholar.org

11^th place

310^th place

1collinsdictionary.com

1,053^rd place

854^th place

1ahdictionary.com

2,334^th place

3,548^th place

1oxforddictionaries.com

710^th place

218^th place

1iupac.org

538^th place

106^th place

1handle.net

102^nd place

307^th place

1ugent.be

3,695^th place

2,391^st place

1books.google.com

3^rd place

9^th place

1uspto.gov

1,459^th place

763^rd place

1pat2pdf.org

low place

2,031^st place

1sigmaaldrich.com

924^th place

265^th place

1ukim.edu.mk

low place

1zenodo.org

621^st place

732^nd place

1nootropicsfrontline.com

low place

ahdictionary.com (Global: 2,334^th place; Korean: 3,548^th place)

“amide” 5판. 《The American Heritage Dictionary of the English Language》. HarperCollins.

archive.org (Global: 6^th place; Korean: 18^th place)

Fletcher, John H. (1974). 〈Chapter 21: Amides and Imides〉. 《Nomenclature of Organic Compounds: Principles and Practice》 126. Washington, DC: American Chemical Society. 166–173쪽. doi:10.1021/ba-1974-0126.ch021. ISBN 9780841201910.
Alan R. Katritzky; Meth-Cohn, Otto; Charles Rees 편집 (1995). 《Comprehensive Organic Functional Group Transformations》 1판 3. Oxford: Pergamon Press. 90쪽. ISBN 0080423248.
Valeur, Eric; Bradley, Mark (2009). “Amide bond formation: beyond the myth of coupling reagents”. 《Chem. Soc. Rev.》 38 (2): 606–631. doi:10.1039/B701677H. PMID 19169468. S2CID 14950926.
Chapman, Arthur William (1925). “CCLXIX.—Imino-aryl ethers. Part III. The molecular rearrangement of N-phenylbenziminophenyl ether”. 《Journal of the Chemical Society, Transactions》 127: 1992–1998. doi:10.1039/CT9252701992.
Gunanathan, C.; Ben-David, Y.; Milstein, D. (2007). “Direct Synthesis of Amides from Alcohols and Amines with Liberation of H₂”. 《Science》 317 (5839): 790–2. Bibcode:2007Sci...317..790G. doi:10.1126/science.1145295. PMID 17690291. S2CID 43671648.

books.google.com (Global: 3^rd place; Korean: 9^th place)

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

collinsdictionary.com (Global: 1,053^rd place; Korean: 854^th place)

“Amide definition and meaning - Collins English Dictionary”. 《www.collinsdictionary.com》. 2018년 4월 15일에 확인함.

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

dx.doi.org

Fletcher, John H. (1974). 〈Chapter 21: Amides and Imides〉. 《Nomenclature of Organic Compounds: Principles and Practice》 126. Washington, DC: American Chemical Society. 166–173쪽. doi:10.1021/ba-1974-0126.ch021. ISBN 9780841201910.
Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart (2012). “Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides” (PDF). 《Journal of Ethnopharmacology》 142 (3): 563–590. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714. PMID 22659196. 2022년 10월 9일에 원본 문서 (PDF)에서 보존된 문서.
Bats, Jan W.; Haberecht, Monika C.; Wagner, Matthias (2003). “A new refinement of the orthorhombic polymorph of acetamide”. 《Acta Crystallographica Section E》 59 (10): o1483–o1485. doi:10.1107/S1600536803019494.
Kemnitz, Carl R.; Loewen, Mark J. (2007). “"Amide Resonance" Correlates with a Breadth of C−N Rotation Barriers”. 《Journal of the American Chemical Society》 129 (9): 2521–8. doi:10.1021/ja0663024. PMID 17295481.
Corson, B. B.; Scott, R. W.; Vose, C. E. (1941). “Cyanoacetamide”. 《Organic Syntheses》 1: 179. doi:10.15227/orgsyn.009.0036.
Jacobs, W. A. (1941). “Chloroacetamide”. 《Organic Syntheses》 1: 153. doi:10.15227/orgsyn.007.0016.
Kleinberg, J.; Audrieth, L. F. (1955). “Lactamide”. 《Organic Syntheses》 3: 516. doi:10.15227/orgsyn.021.0071.
Valeur, Eric; Bradley, Mark (2009). “Amide bond formation: beyond the myth of coupling reagents”. 《Chem. Soc. Rev.》 38 (2): 606–631. doi:10.1039/B701677H. PMID 19169468. S2CID 14950926.
Eller, Karsten; Henkes, Erhard; Rossbacher, Roland; Höke, Hartmut (2000), 〈Amines, Aliphatic〉, 《울만 공업화학 백과사전(Ullmann's Encyclopedia of Industrial Chemistry)》, Weinheim: Wiley-VCH, doi:10.1002/14356007.a02_001.pub2
Wenner, Wilhelm (1952). “Phenylacetamide”. 《Organic Syntheses》 32: 92. doi:10.15227/orgsyn.032.0092.
De Figueiredo, Renata Marcia; Suppo, Jean-Simon; Campagne, Jean-Marc (2016). “Nonclassical Routes for Amide Bond Formation”. 《Chemical Reviews》 116 (19): 12029–12122. doi:10.1021/acs.chemrev.6b00237. PMID 27673596.
Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. (2017년 9월 1일). “Borate esters: Simple catalysts for the sustainable synthesis of complex amides”. 《Science Advances》 3 (9): e1701028. Bibcode:2017SciA....3E1028S. doi:10.1126/sciadv.1701028. PMC 5609808. PMID 28948222.
Schulenberg, J. W.; Archer, S. (1965). “The Chapman Rearrangement”. 《Org. React.》 14: 1–51. doi:10.1002/0471264180.or014.01. ISBN 978-0471264187.
Chapman, Arthur William (1925). “CCLXIX.—Imino-aryl ethers. Part III. The molecular rearrangement of N-phenylbenziminophenyl ether”. 《Journal of the Chemical Society, Transactions》 127: 1992–1998. doi:10.1039/CT9252701992.
Leuckart, R. (1885). “Ueber einige Reaktionen der aromatischen Cyanate”. 《Berichte der deutschen chemischen Gesellschaft》 18: 873–877. doi:10.1002/cber.188501801182.
Adams, Rodger; Krimen, L.I.; Cota, Donald J. (1969). 《Organic Reaction Volume 17》. London: John Wiley & Sons, Inc. 213–326쪽. doi:10.1002/0471264180. ISBN 9780471196150.
Gunanathan, C.; Ben-David, Y.; Milstein, D. (2007). “Direct Synthesis of Amides from Alcohols and Amines with Liberation of H₂”. 《Science》 317 (5839): 790–2. Bibcode:2007Sci...317..790G. doi:10.1126/science.1145295. PMID 17690291. S2CID 43671648.
T. A. Dineen; M. A. Zajac; A. G. Myers (2006). “Efficient Transamidation of Primary Carboxamides by in situ Activation with N,N-Dialkylformamide Dimethyl Acetals”. 《J. Am. Chem. Soc.》 128 (50): 16406–16409. doi:10.1021/ja066728i. PMID 17165798.
Emma L. Baker; Michael M. Yamano; Yujing Zhou; Sarah M. Anthony; Neil K. Garg (2016). “A two-step approach to achieve secondary amide transamidation enabled by nickel catalysis”. 《Nature Communications》 7: 11554. Bibcode:2016NatCo...711554B. doi:10.1038/ncomms11554. PMC 4876455. PMID 27199089.

ghostarchive.org (Global: 32^nd place; Korean: 656^th place)

Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart (2012). “Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides” (PDF). 《Journal of Ethnopharmacology》 142 (3): 563–590. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714. PMID 22659196. 2022년 10월 9일에 원본 문서 (PDF)에서 보존된 문서.
Monson, Richard (1971). 《Advanced Organic Synthesis: Methods and Techniques》 (PDF). New York: Academic Press. 141쪽. ISBN 978-0124336803. 2022년 10월 9일에 원본 문서 (PDF)에서 보존된 문서.

handle.net (Global: 102^nd place; Korean: 307^th place)

hdl.handle.net

Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart (2012). “Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides” (PDF). 《Journal of Ethnopharmacology》 142 (3): 563–590. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714. PMID 22659196. 2022년 10월 9일에 원본 문서 (PDF)에서 보존된 문서.

harvard.edu (Global: 18^th place; Korean: 27^th place)

adsabs.harvard.edu

Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. (2017년 9월 1일). “Borate esters: Simple catalysts for the sustainable synthesis of complex amides”. 《Science Advances》 3 (9): e1701028. Bibcode:2017SciA....3E1028S. doi:10.1126/sciadv.1701028. PMC 5609808. PMID 28948222.
Gunanathan, C.; Ben-David, Y.; Milstein, D. (2007). “Direct Synthesis of Amides from Alcohols and Amines with Liberation of H₂”. 《Science》 317 (5839): 790–2. Bibcode:2007Sci...317..790G. doi:10.1126/science.1145295. PMID 17690291. S2CID 43671648.
Emma L. Baker; Michael M. Yamano; Yujing Zhou; Sarah M. Anthony; Neil K. Garg (2016). “A two-step approach to achieve secondary amide transamidation enabled by nickel catalysis”. 《Nature Communications》 7: 11554. Bibcode:2016NatCo...711554B. doi:10.1038/ncomms11554. PMC 4876455. PMID 27199089.

iupac.org (Global: 538^th place; Korean: 106^th place)

old.iupac.org

틀:BlueBook2004 Full text (PDF) of Draft Rule P-66: Amides, Imides, Hydrazides, Nitriles, Aldehydes, Their Chalcogen Analogues, and Derivatives

nih.gov (Global: 4^th place; Korean: 4^th place)

ncbi.nlm.nih.gov

Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart (2012). “Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides” (PDF). 《Journal of Ethnopharmacology》 142 (3): 563–590. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714. PMID 22659196. 2022년 10월 9일에 원본 문서 (PDF)에서 보존된 문서.
Kemnitz, Carl R.; Loewen, Mark J. (2007). “"Amide Resonance" Correlates with a Breadth of C−N Rotation Barriers”. 《Journal of the American Chemical Society》 129 (9): 2521–8. doi:10.1021/ja0663024. PMID 17295481.
Valeur, Eric; Bradley, Mark (2009). “Amide bond formation: beyond the myth of coupling reagents”. 《Chem. Soc. Rev.》 38 (2): 606–631. doi:10.1039/B701677H. PMID 19169468. S2CID 14950926.
De Figueiredo, Renata Marcia; Suppo, Jean-Simon; Campagne, Jean-Marc (2016). “Nonclassical Routes for Amide Bond Formation”. 《Chemical Reviews》 116 (19): 12029–12122. doi:10.1021/acs.chemrev.6b00237. PMID 27673596.
Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. (2017년 9월 1일). “Borate esters: Simple catalysts for the sustainable synthesis of complex amides”. 《Science Advances》 3 (9): e1701028. Bibcode:2017SciA....3E1028S. doi:10.1126/sciadv.1701028. PMC 5609808. PMID 28948222.
Gunanathan, C.; Ben-David, Y.; Milstein, D. (2007). “Direct Synthesis of Amides from Alcohols and Amines with Liberation of H₂”. 《Science》 317 (5839): 790–2. Bibcode:2007Sci...317..790G. doi:10.1126/science.1145295. PMID 17690291. S2CID 43671648.
T. A. Dineen; M. A. Zajac; A. G. Myers (2006). “Efficient Transamidation of Primary Carboxamides by in situ Activation with N,N-Dialkylformamide Dimethyl Acetals”. 《J. Am. Chem. Soc.》 128 (50): 16406–16409. doi:10.1021/ja066728i. PMID 17165798.
Emma L. Baker; Michael M. Yamano; Yujing Zhou; Sarah M. Anthony; Neil K. Garg (2016). “A two-step approach to achieve secondary amide transamidation enabled by nickel catalysis”. 《Nature Communications》 7: 11554. Bibcode:2016NatCo...711554B. doi:10.1038/ncomms11554. PMC 4876455. PMID 27199089.

nootropicsfrontline.com (Global: low place; Korean: low place)

Monson, Richard (1971). 《Advanced Organic Synthesis: Methods and Techniques》 (PDF). New York: Academic Press. 141쪽. ISBN 978-0124336803. 2022년 10월 9일에 원본 문서 (PDF)에서 보존된 문서.

oxforddictionaries.com (Global: 710^th place; Korean: 218^th place)

“amide - Definition of amide in English by Oxford Dictionaries”. 《Oxford Dictionaries – English》. 2015년 4월 2일에 원본 문서에서 보존된 문서. 2018년 4월 15일에 확인함.

pat2pdf.org (Global: low place; Korean: 2,031^st place)

미국 특허 5,935,953

semanticscholar.org (Global: 11^th place; Korean: 310^th place)

api.semanticscholar.org

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

sigmaaldrich.com (Global: 924^th place; Korean: 265^th place)

“Tris(2,2,2-trifluoroethyl) borate 97% | Sigma-Aldrich”. 《www.sigmaaldrich.com》. 2016년 9월 22일에 확인함.

ugent.be (Global: 3,695^th place; Korean: 2,391^st place)

biblio.ugent.be

Boonen, Jente; Bronselaer, Antoon; Nielandt, Joachim; Veryser, Lieselotte; De Tré, Guy; De Spiegeleer, Bart (2012). “Alkamid database: Chemistry, occurrence and functionality of plant N-alkylamides” (PDF). 《Journal of Ethnopharmacology》 142 (3): 563–590. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714. PMID 22659196. 2022년 10월 9일에 원본 문서 (PDF)에서 보존된 문서.

ukim.edu.mk (Global: low place; Korean: low place)

pmf.ukim.edu.mk

“Bodroux reaction”. Institute of Chemistry, Skopje, Macedonia. 2015년 9월 24일에 원본 문서에서 보존된 문서. 2007년 5월 23일에 확인함.

uspto.gov (Global: 1,459^th place; Korean: 763^rd place)

patft.uspto.gov

미국 특허 5,935,953

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

“amide - Definition of amide in English by Oxford Dictionaries”. 《Oxford Dictionaries – English》. 2015년 4월 2일에 원본 문서에서 보존된 문서. 2018년 4월 15일에 확인함.
“Bodroux reaction”. Institute of Chemistry, Skopje, Macedonia. 2015년 9월 24일에 원본 문서에서 보존된 문서. 2007년 5월 23일에 확인함.

zenodo.org (Global: 621^st place; Korean: 732^nd place)

Leuckart, R. (1885). “Ueber einige Reaktionen der aromatischen Cyanate”. 《Berichte der deutschen chemischen Gesellschaft》 18: 873–877. doi:10.1002/cber.188501801182.

아마이드 (Korean Wikipedia)

ahdictionary.com (Global: 2,334th place; Korean: 3,548th place)

archive.org (Global: 6th place; Korean: 18th place)

books.google.com (Global: 3rd place; Korean: 9th place)

collinsdictionary.com (Global: 1,053rd place; Korean: 854th place)

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

dx.doi.org

ghostarchive.org (Global: 32nd place; Korean: 656th place)

handle.net (Global: 102nd place; Korean: 307th place)

hdl.handle.net

harvard.edu (Global: 18th place; Korean: 27th place)

adsabs.harvard.edu

iupac.org (Global: 538th place; Korean: 106th place)

old.iupac.org

nih.gov (Global: 4th place; Korean: 4th place)

ncbi.nlm.nih.gov

nootropicsfrontline.com (Global: low place; Korean: low place)

oxforddictionaries.com (Global: 710th place; Korean: 218th place)

pat2pdf.org (Global: low place; Korean: 2,031st place)

semanticscholar.org (Global: 11th place; Korean: 310th place)

api.semanticscholar.org

sigmaaldrich.com (Global: 924th place; Korean: 265th place)

ugent.be (Global: 3,695th place; Korean: 2,391st place)

biblio.ugent.be

ukim.edu.mk (Global: low place; Korean: low place)

pmf.ukim.edu.mk

uspto.gov (Global: 1,459th place; Korean: 763rd place)

patft.uspto.gov

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

zenodo.org (Global: 621st place; Korean: 732nd place)

ahdictionary.com (Global: 2,334^th place; Korean: 3,548^th place)

archive.org (Global: 6^th place; Korean: 18^th place)

books.google.com (Global: 3^rd place; Korean: 9^th place)

collinsdictionary.com (Global: 1,053^rd place; Korean: 854^th place)

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

ghostarchive.org (Global: 32^nd place; Korean: 656^th place)

handle.net (Global: 102^nd place; Korean: 307^th place)

harvard.edu (Global: 18^th place; Korean: 27^th place)

iupac.org (Global: 538^th place; Korean: 106^th place)

nih.gov (Global: 4^th place; Korean: 4^th place)

oxforddictionaries.com (Global: 710^th place; Korean: 218^th place)

pat2pdf.org (Global: low place; Korean: 2,031^st place)

semanticscholar.org (Global: 11^th place; Korean: 310^th place)

sigmaaldrich.com (Global: 924^th place; Korean: 265^th place)

ugent.be (Global: 3,695^th place; Korean: 2,391^st place)

uspto.gov (Global: 1,459^th place; Korean: 763^rd place)

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

zenodo.org (Global: 621^st place; Korean: 732^nd place)