Anhidrid organske kiseline (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Anhidrid organske kiseline" in Serbian language version.

refsWebsite

Global rank Serbian rank

11doi.org

2^nd place

4^th place

3nih.gov

4^th place

8^th place

2libretexts.org

3,627^th place

3,244^th place

2harvard.edu

18^th place

28^th place

1iupac.org

538^th place

222^nd place

1acdlabs.com

low place

3,594^th place

1orgsyn.org

2,971^st place

2,328^th place

1wiley.com

222^nd place

155^th place

1worldcat.org

5^th place

12^th place

1bris.ac.uk

4,848^th place

5,026^th place

1semanticscholar.org

11^th place

23^rd place

1wikipedia.org

low place

1handle.net

102^nd place

266^th place

1ox.ac.uk

613^th place

779^th place

acdlabs.com

IUPAC, A Guide to IUPAC Nomenclature of Organic Compounds (the Blue Book); Oxford: Blackwell Science (1993). ISBN 0-632-03488-2. Online edition: "Recommendation R-R-5.7.7.". pp. 123–25.

bris.ac.uk

research-information.bris.ac.uk

Heard, David M.; Tayler, Emyr R.; Cox, Russell J.; Simpson, Thomas J.; Willis, Christine L. (3. 1. 2020). „Structural and synthetic studies on maleic anhydride and related diacid natural products” (PDF). Tetrahedron. 76 (1): 130717. S2CID 209714625. doi:10.1016/j.tet.2019.130717. hdl:1983/53998d06-9017-4cfb-822b-c6453348000a.

doi.org

Zoeller, Joseph R.; Agreda, Victor H.; Cook, Steven L.; Lafferty, Norma L.; Polichnowski, Stanley W.; Pond, David M. (1992). „Eastman chemical company acetic anhydride process”. Catalysis Today. 13: 73—91. doi:10.1016/0920-5861(92)80188-S.
Heimo Held; Alfred Rengstl; Dieter Mayer (2002). "Acetic Anhydride and Mixed Fatty Acid Anhydrides" Ullmann's Encyclopedia of Industrial Chemistry. Wiley-VCH, Weinheim. doi:10.1002/14356007.a01_065.
Chiang, Wen-Yen; Chiang, Wen-Chang (05. 05. 1988). „Condensation polymerization of multifunctional monomers and properties of related polyester resins. II. Thermal properties of polyester—imide varnishes”. Journal of Applied Polymer Science. 35 (6): 1433—1439. doi:10.1002/app.1988.070350603.
Faghihi, Khalil; Ashouri, Mostafa; Hajibeygi, Mohsen (25. 10. 2013). „High Temperature and Organosoluble Poly(amide-imide)s Based on 1,4-Bis[4-aminophenoxy]butane and Aromatic Diacids by Direct Polycondensation: Synthesis and Properties”. High Temperature Materials and Processes (на језику: енглески). 32 (5): 451—458. ISSN 2191-0324. doi:10.1515/htmp-2012-0164 .
Saleem, Muhammad; Hussain, Hidayat; Ahmed, Ishtiaq; Draeger, Siegfried; Schulz, Barbara; Meier, Kathrin; Steinert, Michael; Pescitelli, Gennaro; Kurtán, Tibor; Flörke, Ulrich; Krohn, Karsten (фебруар 2011). „Viburspiran, an Antifungal Member of the Octadride Class of Maleic Anhydride Natural Products”. European Journal of Organic Chemistry. 2011 (4): 808—812. doi:10.1002/ejoc.201001324.
Han, Chunguang; Furukawa, Hiroyuki; Tomura, Tomohiko; Fudou, Ryosuke; Kaida, Kenichi; Choi, Bong-Keun; Imokawa, Genji; Ojika, Makoto (24. 4. 2015). „Bioactive Maleic Anhydrides and Related Diacids from the Aquatic Hyphomycete Tricladium castaneicola”. Journal of Natural Products. 78 (4): 639—644. PMID 25875311. doi:10.1021/np500773s.
Heard, David M.; Tayler, Emyr R.; Cox, Russell J.; Simpson, Thomas J.; Willis, Christine L. (3. 1. 2020). „Structural and synthetic studies on maleic anhydride and related diacid natural products” (PDF). Tetrahedron. 76 (1): 130717. S2CID 209714625. doi:10.1016/j.tet.2019.130717. hdl:1983/53998d06-9017-4cfb-822b-c6453348000a.
Chen, Xiaolong; Zheng, Yuguo; Shen, Yinchu (мај 2007). „Natural Products with Maleic Anhydride Structure: Nonadrides, Tautomycin, Chaetomellic Anhydride, and Other Compounds”. Chemical Reviews. 107 (5): 1777—1830. PMID 17439289. doi:10.1021/cr050029r.
Kuban, Vojtech (2020). „Structural Basis of Ca 2+-Dependent Self-Processing Activity of Repeat-in-Toxin Proteins”. mBio. 11 (2): e00226—20. doi:10.1128/mBio.00226-20.
Bell, Christian (2013). „Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub”. Science. 341 (6141): 77—80. Bibcode:2013Sci...341...77B. PMC 4730555 . PMID 23744777. doi:10.1126/science.1232322.
Scheu, Arne (2021). „NeissLock provides an inducible protein anhydride for covalent targeting of endogenous proteins” (PDF). Nature Communications. 12 (1): 717. Bibcode:2021NatCo..12..717S. doi:10.1038/s41467-021-20963-5.

handle.net

hdl.handle.net

Heard, David M.; Tayler, Emyr R.; Cox, Russell J.; Simpson, Thomas J.; Willis, Christine L. (3. 1. 2020). „Structural and synthetic studies on maleic anhydride and related diacid natural products” (PDF). Tetrahedron. 76 (1): 130717. S2CID 209714625. doi:10.1016/j.tet.2019.130717. hdl:1983/53998d06-9017-4cfb-822b-c6453348000a.

harvard.edu

adsabs.harvard.edu

Bell, Christian (2013). „Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub”. Science. 341 (6141): 77—80. Bibcode:2013Sci...341...77B. PMC 4730555 . PMID 23744777. doi:10.1126/science.1232322.
Scheu, Arne (2021). „NeissLock provides an inducible protein anhydride for covalent targeting of endogenous proteins” (PDF). Nature Communications. 12 (1): 717. Bibcode:2021NatCo..12..717S. doi:10.1038/s41467-021-20963-5.

iupac.org

goldbook.iupac.org

IUPAC. „acid anhydrides”. Kompendijum hemijske terminologije (Internet izdanje).

libretexts.org

chem.libretexts.org

„Nomenclature of Anhydrides”. 8. 11. 2013.
„Nomenclature of Anhydrides”. 8. 11. 2013.

nih.gov

ncbi.nlm.nih.gov

Han, Chunguang; Furukawa, Hiroyuki; Tomura, Tomohiko; Fudou, Ryosuke; Kaida, Kenichi; Choi, Bong-Keun; Imokawa, Genji; Ojika, Makoto (24. 4. 2015). „Bioactive Maleic Anhydrides and Related Diacids from the Aquatic Hyphomycete Tricladium castaneicola”. Journal of Natural Products. 78 (4): 639—644. PMID 25875311. doi:10.1021/np500773s.
Chen, Xiaolong; Zheng, Yuguo; Shen, Yinchu (мај 2007). „Natural Products with Maleic Anhydride Structure: Nonadrides, Tautomycin, Chaetomellic Anhydride, and Other Compounds”. Chemical Reviews. 107 (5): 1777—1830. PMID 17439289. doi:10.1021/cr050029r.
Bell, Christian (2013). „Structure of the repulsive guidance molecule (RGM)-neogenin signaling hub”. Science. 341 (6141): 77—80. Bibcode:2013Sci...341...77B. PMC 4730555 . PMID 23744777. doi:10.1126/science.1232322.

orgsyn.org

Lewis I. Krimen (1988). „Acetic Formic Anhydride”. Org. Synth. ; Coll. Vol., 6, стр. 8

ox.ac.uk

ora.ox.ac.uk

Scheu, Arne (2021). „NeissLock provides an inducible protein anhydride for covalent targeting of endogenous proteins” (PDF). Nature Communications. 12 (1): 717. Bibcode:2021NatCo..12..717S. doi:10.1038/s41467-021-20963-5.

semanticscholar.org

api.semanticscholar.org

Heard, David M.; Tayler, Emyr R.; Cox, Russell J.; Simpson, Thomas J.; Willis, Christine L. (3. 1. 2020). „Structural and synthetic studies on maleic anhydride and related diacid natural products” (PDF). Tetrahedron. 76 (1): 130717. S2CID 209714625. doi:10.1016/j.tet.2019.130717. hdl:1983/53998d06-9017-4cfb-822b-c6453348000a.

wikipedia.org

en.wikipedia.org

Heard, David M.; Tayler, Emyr R.; Cox, Russell J.; Simpson, Thomas J.; Willis, Christine L. (3. 1. 2020). „Structural and synthetic studies on maleic anhydride and related diacid natural products” (PDF). Tetrahedron. 76 (1): 130717. S2CID 209714625. doi:10.1016/j.tet.2019.130717. hdl:1983/53998d06-9017-4cfb-822b-c6453348000a.

wiley.com

onlinelibrary.wiley.com

Chiang, Wen-Yen; Chiang, Wen-Chang (05. 05. 1988). „Condensation polymerization of multifunctional monomers and properties of related polyester resins. II. Thermal properties of polyester—imide varnishes”. Journal of Applied Polymer Science. 35 (6): 1433—1439. doi:10.1002/app.1988.070350603.

worldcat.org

Faghihi, Khalil; Ashouri, Mostafa; Hajibeygi, Mohsen (25. 10. 2013). „High Temperature and Organosoluble Poly(amide-imide)s Based on 1,4-Bis[4-aminophenoxy]butane and Aromatic Diacids by Direct Polycondensation: Synthesis and Properties”. High Temperature Materials and Processes (на језику: енглески). 32 (5): 451—458. ISSN 2191-0324. doi:10.1515/htmp-2012-0164 .