Amid (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Amid" in Serbian language version.

refsWebsite

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16doi.org

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6nih.gov

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3web.archive.org

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3archive.org

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3sigmaaldrich.com

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3harvard.edu

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2iupac.org

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1collinsdictionary.com

1,053^rd place

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1oxforddictionaries.com

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1organic-chemistry.org

low place

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1acdlabs.com

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1ugent.be

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1wikipedia.org

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1handle.net

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1ukim.edu.mk

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acdlabs.com

Organic Chemistry IUPAC Nomenclature. Rules C-821. Amides http://www.acdlabs.com/iupac/nomenclature/79/r79_540.htm Архивирано 2011-01-21 на сајту Wayback Machine

archive.org

Valeur, Eric; Bradley, Mark (2009). „Amide bond formation: beyond the myth of coupling reagents”. Chem. Soc. Rev. 38 (2): 606—631. PMID 19169468. doi:10.1039/B701677H.
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.
Monson, Richard (1971). Advanced Organic Synthesis: Methods and Techniques. Newyork: Academic Press. стр. 141. ISBN 978-0124336803.

collinsdictionary.com

„Amide definition and meaning - Collins English Dictionary”. www.collinsdictionary.com. Приступљено 15. 4. 2018.

doi.org

„Chemistry International”. Chemistry International. 29 (4). 2007. doi:10.1515/ci.2007.29.4.16.
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. PMID 17295481. doi:10.1021/ja0663024.
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—90. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714.
Montalbetti, Christian A. G. N.; Falque, Virginie (14. 11. 2005). „Amide bond formation and peptide coupling”. Tetrahedron. 61 (46): 10827—10852. doi:10.1016/j.tet.2005.08.031.
Valeur, Eric; Bradley, Mark (2009). „Amide bond formation: beyond the myth of coupling reagents”. Chem. Soc. Rev. 38 (2): 606—631. PMID 19169468. doi:10.1039/B701677H.
Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. (1. 9. 2017). „Borate esters: Simple catalysts for the sustainable synthesis of complex amides”. Science Advances. 3 (9): e1701028. Bibcode:2017SciA....3E1028S. PMC 5609808 . PMID 28948222. doi:10.1126/sciadv.1701028.
Schulenberg, J. W.; Archer, S. (1965). The Chapman Rearrangement. Org. React. 14. стр. 1—51. ISBN 978-0471264187. doi:10.1002/0471264180.or014.01.
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. стр. 213—326. ISBN 9780471196150. doi:10.1002/0471264180.
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.
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. PMID 17690291. doi:10.1126/science.1145295.
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.
Emma L. Baker; Michael M. Yamano; Zhou, Yujing; 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. PMC 4876455 . PMID 27199089. doi:10.1038/ncomms11554.

handle.net

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—90. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714.

harvard.edu

adsabs.harvard.edu

Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. (1. 9. 2017). „Borate esters: Simple catalysts for the sustainable synthesis of complex amides”. Science Advances. 3 (9): e1701028. Bibcode:2017SciA....3E1028S. PMC 5609808 . PMID 28948222. doi:10.1126/sciadv.1701028.
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. PMID 17690291. doi:10.1126/science.1145295.
Emma L. Baker; Michael M. Yamano; Zhou, Yujing; 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. PMC 4876455 . PMID 27199089. doi:10.1038/ncomms11554.

iupac.org

goldbook.iupac.org

IUPAC. „amides”. Kompendijum hemijske terminologije (Internet izdanje).

old2015.iupac.org

„Chemistry International”. Chemistry International. 29 (4). 2007. doi:10.1515/ci.2007.29.4.16.

nih.gov

ncbi.nlm.nih.gov

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. PMID 17295481. doi:10.1021/ja0663024.
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—90. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714.
Valeur, Eric; Bradley, Mark (2009). „Amide bond formation: beyond the myth of coupling reagents”. Chem. Soc. Rev. 38 (2): 606—631. PMID 19169468. doi:10.1039/B701677H.
Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. (1. 9. 2017). „Borate esters: Simple catalysts for the sustainable synthesis of complex amides”. Science Advances. 3 (9): e1701028. Bibcode:2017SciA....3E1028S. PMC 5609808 . PMID 28948222. doi:10.1126/sciadv.1701028.
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. PMID 17690291. doi:10.1126/science.1145295.
Emma L. Baker; Michael M. Yamano; Zhou, Yujing; 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. PMC 4876455 . PMID 27199089. doi:10.1038/ncomms11554.

organic-chemistry.org

Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (I изд.). Oxford University Press. ISBN 978-0-19-850346-0.

oxforddictionaries.com

„amide - Definition of amide in English by Oxford Dictionaries”. Oxford Dictionaries - English. Архивирано из оригинала 20. 08. 2016. г. Приступљено 15. 4. 2018.

sigmaaldrich.com

„Greener Methods: Catalytic Amide Bond Formation”. Приступљено 22. 9. 2016.
„MIBA 96% | Sigma-Aldrich”. www.sigmaaldrich.com. Приступљено 22. 9. 2016.
„Tris(2,2,2-trifluoroethyl) borate 97% | Sigma-Aldrich”. www.sigmaaldrich.com. Приступљено 22. 9. 2016.

ugent.be

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—90. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714.

ukim.edu.mk

pmf.ukim.edu.mk

„Bodroux reaction”. Institute of Chemistry, Skopje, Macedonia. Архивирано из оригинала 24. 09. 2015. г. Приступљено 16. 10. 2019.

web.archive.org

„amide - Definition of amide in English by Oxford Dictionaries”. Oxford Dictionaries - English. Архивирано из оригинала 20. 08. 2016. г. Приступљено 15. 4. 2018.
Organic Chemistry IUPAC Nomenclature. Rules C-821. Amides http://www.acdlabs.com/iupac/nomenclature/79/r79_540.htm Архивирано 2011-01-21 на сајту Wayback Machine
„Bodroux reaction”. Institute of Chemistry, Skopje, Macedonia. Архивирано из оригинала 24. 09. 2015. г. Приступљено 16. 10. 2019.

wikipedia.org

en.wikipedia.org

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—90. PMID 22659196. doi:10.1016/j.jep.2012.05.038. hdl:1854/LU-2133714.