Tioester (Indonesian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Tioester" in Indonesian language version.

Last modified: 14:48:33, 16 August 2026 (UTC)

Ref.Un. Ref.Website

Global rank Indonesian rank

1613doi.org

2^nd place

77nih.gov

5^th place

6^th place

44semanticscholar.org

15^th place

26^th place

33archive.org

6^th place

3^rd place

11organic-chemistry.org

low place

11orgsyn.org

3,535^th place

1,969^th place

11zenodo.org

737^th place

584^th place

11worldcat.org

4^th place

5^th place

archive.org (Global: 6^th place; Indonesian: 3^rd place)

Volante, R. (1981). "A new, highly efficient method for the conversion of alcohols to thiolesters and thiols". Tetrahedron Letters. 22 (33): 3119–3122. doi:10.1016/S0040-4039(01)81842-6.
Lehninger, A. L.; Nelson, D. L.; Cox, M. M. (2000). Principles of Biochemistry (Edisi 3rd). New York: Worth Publishing. ISBN 1-57259-153-6.
Cremlyn, R. J. (1996). An Introduction to Organosulfur Chemistry. Chichester: John Wiley and Sons. ISBN 0-471-95512-4.

doi.org (Global: 2^nd place; Indonesian: 2^nd place)

Matthys J. Janssen (1969). "Thiolo, Thiono and Dithio Acids and Esters". Dalam Saul Patai (ed.). Carboxylic Acids and Esters. PATAI's Chemistry of Functional Groups. New York: John Wiley. hlm. 705–764. doi:10.1002/9780470771099.ch15.
Fujiwara, S.; Kambe, N. (2005). "Thio-, Seleno-, and Telluro-Carboxylic Acid Esters". Topics in Current Chemistry. Vol. 251. Berlin / Heidelberg: Springer. hlm. 87–140. doi:10.1007/b101007. ISBN 978-3-540-23012-0.
Jordan, Andrew; Sneddon, Helen F. (2019). "Development of a solvent-reagent selection guide for the formation of thioesters". Green Chemistry. 21 (8): 1900–1906. doi:10.1039/C9GC00355J. S2CID 107391323.
Volante, R. (1981). "A new, highly efficient method for the conversion of alcohols to thiolesters and thiols". Tetrahedron Letters. 22 (33): 3119–3122. doi:10.1016/S0040-4039(01)81842-6.
Bertleff, W.; Roeper, M.; Sava, X. (2005), "Carbonylation", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a05_217.pub2 {{citation}}: Kutipan memiliki paramater tidak diketahui : |authors=
McGrath, N. A.; Raines, R. T. (2011). "Chemoselectivity in chemical biology: Acyl transfer reactions with sulfur and selenium". Acc. Chem. Res. 44 (9): 752–761. doi:10.1021/ar200081s. PMC 3242736. PMID 21639109.
Wan Kit Chan; S. Masamune; Gary O. Spessard (1983). "Preparation of O-esters From The Corresponding Thiol Esters: tert-butyl Cyclohexanecarboxylate". Organic Syntheses. 61: 48. doi:10.15227/orgsyn.061.0048.{{cite journal}}: Pemeliharaan CS1: DOI bebas tanpa ditandai (link)
Matteo Minozzi; Daniele Nanni; Piero Spagnolo (2008). "4-Pentyne-1-thiol". EEROS. doi:10.1002/047084289X.rn00855. ISBN 978-0-471-93623-7.{{cite journal}}: Pemeliharaan CS1: terbitan berkala memiliki ISBN (link)
Mansuy, D.; Dansette, P. M. (2011). "Sulfenic acids as reactive intermediates in xenobiotic metabolism". Archives of Biochemistry and Biophysics. 507 (1): 174–185. doi:10.1016/j.abb.2010.09.015. PMID 20869346.
Dansette, P. M.; Rosi, J.; Debernardi, J.; Bertho, G.; Mansuy, D. (2012). "Metabolic Activation of Prasugrel: Nature of the Two Competitive Pathways Resulting in the Opening of Its Thiophene Ring". Chemical Research in Toxicology. 25 (5): 1058–1065. doi:10.1021/tx3000279. PMID 22482514.
Newton, Josiah J.; Britton, Robert; Friesen, Chadron M. (4 Oktober 2018). "Base-Catalyzed Transesterification of Thionoesters". The Journal of Organic Chemistry. 83 (20): 12784–12792. doi:10.1021/acs.joc.8b02260. PMID 30235418. S2CID 52309850.{{cite journal}}: Pemeliharaan CS1: Tanggal diterjemahkan otomatis (link)
Monteith, John J.; Scotchburn, Katerina; Mills, L. Reginald; Rousseaux, Sophie A. L. (2022). "Ni-Catalyzed Synthesis of Thiocarboxylic Acid Derivatives". Organic Letters. 24 (2): 619–624. doi:10.1021/acs.orglett.1c04074. PMID 34978834. S2CID 245669904.
Liu, Yinbo; Mo, Xiaofeng; Majeed, Irfan; Zhang, Mei; Wang, Hui; Zeng, Zhuo (2022). "An efficient and straightforward approach for accessing thionoesters via palladium-catalyzed C–N cleavage of thioamides". Organic & Biomolecular Chemistry. 20 (7): 1532–1537. doi:10.1039/d1ob02349g. ISSN 1477-0520. PMID 35129563. S2CID 246418140.

nih.gov (Global: 5^th place; Indonesian: 6^th place)

pubmed.ncbi.nlm.nih.gov

McGrath, N. A.; Raines, R. T. (2011). "Chemoselectivity in chemical biology: Acyl transfer reactions with sulfur and selenium". Acc. Chem. Res. 44 (9): 752–761. doi:10.1021/ar200081s. PMC 3242736. PMID 21639109.
Mansuy, D.; Dansette, P. M. (2011). "Sulfenic acids as reactive intermediates in xenobiotic metabolism". Archives of Biochemistry and Biophysics. 507 (1): 174–185. doi:10.1016/j.abb.2010.09.015. PMID 20869346.
Dansette, P. M.; Rosi, J.; Debernardi, J.; Bertho, G.; Mansuy, D. (2012). "Metabolic Activation of Prasugrel: Nature of the Two Competitive Pathways Resulting in the Opening of Its Thiophene Ring". Chemical Research in Toxicology. 25 (5): 1058–1065. doi:10.1021/tx3000279. PMID 22482514.
Newton, Josiah J.; Britton, Robert; Friesen, Chadron M. (4 Oktober 2018). "Base-Catalyzed Transesterification of Thionoesters". The Journal of Organic Chemistry. 83 (20): 12784–12792. doi:10.1021/acs.joc.8b02260. PMID 30235418. S2CID 52309850.{{cite journal}}: Pemeliharaan CS1: Tanggal diterjemahkan otomatis (link)
Monteith, John J.; Scotchburn, Katerina; Mills, L. Reginald; Rousseaux, Sophie A. L. (2022). "Ni-Catalyzed Synthesis of Thiocarboxylic Acid Derivatives". Organic Letters. 24 (2): 619–624. doi:10.1021/acs.orglett.1c04074. PMID 34978834. S2CID 245669904.
Liu, Yinbo; Mo, Xiaofeng; Majeed, Irfan; Zhang, Mei; Wang, Hui; Zeng, Zhuo (2022). "An efficient and straightforward approach for accessing thionoesters via palladium-catalyzed C–N cleavage of thioamides". Organic & Biomolecular Chemistry. 20 (7): 1532–1537. doi:10.1039/d1ob02349g. ISSN 1477-0520. PMID 35129563. S2CID 246418140.

ncbi.nlm.nih.gov

McGrath, N. A.; Raines, R. T. (2011). "Chemoselectivity in chemical biology: Acyl transfer reactions with sulfur and selenium". Acc. Chem. Res. 44 (9): 752–761. doi:10.1021/ar200081s. PMC 3242736. PMID 21639109.

organic-chemistry.org (Global: low place; Indonesian: low place)

"Synthesis of thioesters". Organic Chemistry Portal.

orgsyn.org (Global: 3,535^th place; Indonesian: 1,969^th place)

(2007) "Synthesis of Multifunctionalized Ketones Through the Fukuyama Coupling Reaction Catalyzed by Pearlman's Catalyst: Preparation of Ethyl 6-oxotridecanoate". Org. Synth. 84: 285; Coll. Vol. 11: 281.

semanticscholar.org (Global: 15^th place; Indonesian: 26^th place)

api.semanticscholar.org

Jordan, Andrew; Sneddon, Helen F. (2019). "Development of a solvent-reagent selection guide for the formation of thioesters". Green Chemistry. 21 (8): 1900–1906. doi:10.1039/C9GC00355J. S2CID 107391323.
Newton, Josiah J.; Britton, Robert; Friesen, Chadron M. (4 Oktober 2018). "Base-Catalyzed Transesterification of Thionoesters". The Journal of Organic Chemistry. 83 (20): 12784–12792. doi:10.1021/acs.joc.8b02260. PMID 30235418. S2CID 52309850.{{cite journal}}: Pemeliharaan CS1: Tanggal diterjemahkan otomatis (link)
Monteith, John J.; Scotchburn, Katerina; Mills, L. Reginald; Rousseaux, Sophie A. L. (2022). "Ni-Catalyzed Synthesis of Thiocarboxylic Acid Derivatives". Organic Letters. 24 (2): 619–624. doi:10.1021/acs.orglett.1c04074. PMID 34978834. S2CID 245669904.
Liu, Yinbo; Mo, Xiaofeng; Majeed, Irfan; Zhang, Mei; Wang, Hui; Zeng, Zhuo (2022). "An efficient and straightforward approach for accessing thionoesters via palladium-catalyzed C–N cleavage of thioamides". Organic & Biomolecular Chemistry. 20 (7): 1532–1537. doi:10.1039/d1ob02349g. ISSN 1477-0520. PMID 35129563. S2CID 246418140.

worldcat.org (Global: 4^th place; Indonesian: 5^th place)

search.worldcat.org

Liu, Yinbo; Mo, Xiaofeng; Majeed, Irfan; Zhang, Mei; Wang, Hui; Zeng, Zhuo (2022). "An efficient and straightforward approach for accessing thionoesters via palladium-catalyzed C–N cleavage of thioamides". Organic & Biomolecular Chemistry. 20 (7): 1532–1537. doi:10.1039/d1ob02349g. ISSN 1477-0520. PMID 35129563. S2CID 246418140.

zenodo.org (Global: 737^th place; Indonesian: 584^th place)

Mansuy, D.; Dansette, P. M. (2011). "Sulfenic acids as reactive intermediates in xenobiotic metabolism". Archives of Biochemistry and Biophysics. 507 (1): 174–185. doi:10.1016/j.abb.2010.09.015. PMID 20869346.

Tioester (Indonesian Wikipedia)

archive.org (Global: 6th place; Indonesian: 3rd place)

doi.org (Global: 2nd place; Indonesian: 2nd place)

nih.gov (Global: 5th place; Indonesian: 6th place)