Disulfide (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Disulfide" in English language version.

Last modified: 00:55:42, 12 September 2026 (UTC)

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1613doi.org

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55nih.gov

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33semanticscholar.org

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31sciencedirect.com

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22adsabs.harvard.edu

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11interchim.fr

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acs.org (Global: 865^th place; English: 887^th place)

pubs.acs.org

Kreitman, Gal Y. (March 5, 2017). "Copper(II)-Mediated Hydrogen Sulfide and Thiol Oxidation to Disulfides and Organic Polysulfanes and Their Reductive Cleavage in Wine: Mechanistic Elucidation and Potential Applications". Journal of Agricultural and Food Chemistry. 65 (12): 2564–2571. Bibcode:2017JAFC...65.2564K. doi:10.1021/acs.jafc.6b05418. PMID 28260381. Retrieved 31 May 2021.

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

ui.adsabs.harvard.edu

Lee, J. D.; Bryant, M. W. R. (1969). "The Crystal Structure of Diphenyl Disulphide". Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 25 (10): 2094–2101. Bibcode:1969AcCrB..25.2094L. doi:10.1107/S0567740869005188.
Kreitman, Gal Y. (March 5, 2017). "Copper(II)-Mediated Hydrogen Sulfide and Thiol Oxidation to Disulfides and Organic Polysulfanes and Their Reductive Cleavage in Wine: Mechanistic Elucidation and Potential Applications". Journal of Agricultural and Food Chemistry. 65 (12): 2564–2571. Bibcode:2017JAFC...65.2564K. doi:10.1021/acs.jafc.6b05418. PMID 28260381. Retrieved 31 May 2021.

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

Lee, J. D.; Bryant, M. W. R. (1969). "The Crystal Structure of Diphenyl Disulphide". Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry. 25 (10): 2094–2101. Bibcode:1969AcCrB..25.2094L. doi:10.1107/S0567740869005188.
Houk, Janette; Whitesides, George M. (1989). "Characterization and stability of cyclic disulfides and cyclic dimeric bis(disulfides)". Tetrahedron. 45: 91–102. doi:10.1016/0040-4020(89)80036-5.
Sevier, C. S.; Kaiser, C. A. (2002). "Formation and transfer of disulphide bonds in living cells". Nature Reviews Molecular Cell Biology. 3 (11): 836–847. doi:10.1038/nrm954. PMID 12415301. S2CID 2885059.
Witt, D. (2008). "Recent developments in disulfide bond formation". Synthesis. 2008 (16): 2491–2509. doi:10.1055/s-2008-1067188.
Kreitman, Gal Y. (March 5, 2017). "Copper(II)-Mediated Hydrogen Sulfide and Thiol Oxidation to Disulfides and Organic Polysulfanes and Their Reductive Cleavage in Wine: Mechanistic Elucidation and Potential Applications". Journal of Agricultural and Food Chemistry. 65 (12): 2564–2571. Bibcode:2017JAFC...65.2564K. doi:10.1021/acs.jafc.6b05418. PMID 28260381. Retrieved 31 May 2021.
M. E. Alonso; H. Aragona (1978). "Sulfide Synthesis in Preparation of Unsymmetrical Dialkyl Disulfides: sec-Butyl Isopropyl Disulfide". Org. Synth. 58: 147. doi:10.15227/orgsyn.058.0147.
- Hubacher, Max H. (1935). "o-Nitrophenylsulfur Chloride". Organic Syntheses. 15: 45. doi:10.15227/orgsyn.015.00452
- Nikolai S. Zefirov; Nikolai V. Zyk; Elena K. Beloglazkina; Andrei G. Kutateladze (1993). "Thiosulfonates: Synthesis, Reactions and Practical Applications". Sulfur Reports. 14: 223–240. doi:10.1080/01961779308055018.
- Gilbert, H. F. (1990). "Molecular and Cellular Aspects of Thiol–Disulfide Exchange". Advances in Enzymology and Related Areas of Molecular Biology. Vol. 63. pp. 69–172. doi:10.1002/9780470123096.ch2. ISBN 978-0-470-12309-6. PMID 2407068.
- Gilbert, H. F. (1995). "Thiol/disulfide exchange equilibria and disulfide bond stability". Biothiols, Part A: Monothiols and Dithiols, Protein Thiols, and Thiyl Radicals. Methods in Enzymology. Vol. 251. pp. 8–28. doi:10.1016/0076-6879(95)51107-5. ISBN 978-0-12-182152-4. PMID 7651233.
- Akiba, M.; Hashim, A.S. (1997). "Vulcanization and crosslinking in elastomers". Progress in Polymer Science. 22 (3): 475–521. doi:10.1016/S0079-6700(96)00015-9 – via Elsevier Science Direct.
- Mutlu, Hatice; Theato, Patrick (2020). "Making the Best of Polymers with Sulfur–Nitrogen Bonds: From Sources to Innovative Materials". Macromolecular Rapid Communications. 41 (13) 2000181. doi:10.1002/marc.202000181. PMID 32462759. S2CID 218975603.
- Bin Rusayyis, Mohammed; Torkelson, John (2021). "Reprocessable covalent adaptable networks with excellent elevated-temperature creep resistance: facilitation by dynamic, dissociative bis(hindered amino) disulfide bonds". Polymer Chemistry. 12 (18): 2760–2771. doi:10.1039/D1PY00187F. S2CID 234925061.
interchim.fr (Global: low place; English: low place)
- TCEP technical information, from Interchim
nih.gov (Global: 5^th place; English: 5^th place)
pubmed.ncbi.nlm.nih.gov
- Sevier, C. S.; Kaiser, C. A. (2002). "Formation and transfer of disulphide bonds in living cells". Nature Reviews Molecular Cell Biology. 3 (11): 836–847. doi:10.1038/nrm954. PMID 12415301. S2CID 2885059.
- Kreitman, Gal Y. (March 5, 2017). "Copper(II)-Mediated Hydrogen Sulfide and Thiol Oxidation to Disulfides and Organic Polysulfanes and Their Reductive Cleavage in Wine: Mechanistic Elucidation and Potential Applications". Journal of Agricultural and Food Chemistry. 65 (12): 2564–2571. Bibcode:2017JAFC...65.2564K. doi:10.1021/acs.jafc.6b05418. PMID 28260381. Retrieved 31 May 2021.
- Gilbert, H. F. (1990). "Molecular and Cellular Aspects of Thiol–Disulfide Exchange". Advances in Enzymology and Related Areas of Molecular Biology. Vol. 63. pp. 69–172. doi:10.1002/9780470123096.ch2. ISBN 978-0-470-12309-6. PMID 2407068.
- Gilbert, H. F. (1995). "Thiol/disulfide exchange equilibria and disulfide bond stability". Biothiols, Part A: Monothiols and Dithiols, Protein Thiols, and Thiyl Radicals. Methods in Enzymology. Vol. 251. pp. 8–28. doi:10.1016/0076-6879(95)51107-5. ISBN 978-0-12-182152-4. PMID 7651233.
- Mutlu, Hatice; Theato, Patrick (2020). "Making the Best of Polymers with Sulfur–Nitrogen Bonds: From Sources to Innovative Materials". Macromolecular Rapid Communications. 41 (13) 2000181. doi:10.1002/marc.202000181. PMID 32462759. S2CID 218975603.
rsc.org (Global: 2,104^th place; English: 1,855^th place)
pubs.rsc.org
- Bin Rusayyis, Mohammed; Torkelson, John (2021). "Reprocessable covalent adaptable networks with excellent elevated-temperature creep resistance: facilitation by dynamic, dissociative bis(hindered amino) disulfide bonds". Polymer Chemistry. 12 (18): 2760–2771. doi:10.1039/D1PY00187F. S2CID 234925061.
sciencedirect.com (Global: 137^th place; English: 146^th place)
- Akiba, M.; Hashim, A.S. (1997). "Vulcanization and crosslinking in elastomers". Progress in Polymer Science. 22 (3): 475–521. doi:10.1016/S0079-6700(96)00015-9 – via Elsevier Science Direct.
semanticscholar.org (Global: 15^th place; English: 8^th place)
api.semanticscholar.org
- Sevier, C. S.; Kaiser, C. A. (2002). "Formation and transfer of disulphide bonds in living cells". Nature Reviews Molecular Cell Biology. 3 (11): 836–847. doi:10.1038/nrm954. PMID 12415301. S2CID 2885059.
- Mutlu, Hatice; Theato, Patrick (2020). "Making the Best of Polymers with Sulfur–Nitrogen Bonds: From Sources to Innovative Materials". Macromolecular Rapid Communications. 41 (13) 2000181. doi:10.1002/marc.202000181. PMID 32462759. S2CID 218975603.
- Bin Rusayyis, Mohammed; Torkelson, John (2021). "Reprocessable covalent adaptable networks with excellent elevated-temperature creep resistance: facilitation by dynamic, dissociative bis(hindered amino) disulfide bonds". Polymer Chemistry. 12 (18): 2760–2771. doi:10.1039/D1PY00187F. S2CID 234925061.

Disulfide (English Wikipedia)

acs.org (Global: 865th place; English: 887th place)

pubs.acs.org

adsabs.harvard.edu (Global: 14th place; English: 9th place)

ui.adsabs.harvard.edu

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

interchim.fr (Global: low place; English: low place)

nih.gov (Global: 5th place; English: 5th place)

pubmed.ncbi.nlm.nih.gov

rsc.org (Global: 2,104th place; English: 1,855th place)

pubs.rsc.org

sciencedirect.com (Global: 137th place; English: 146th place)

semanticscholar.org (Global: 15th place; English: 8th place)

api.semanticscholar.org

acs.org (Global: 865^th place; English: 887^th place)

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

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

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

rsc.org (Global: 2,104^th place; English: 1,855^th place)

sciencedirect.com (Global: 137^th place; English: 146^th place)

semanticscholar.org (Global: 15^th place; English: 8^th place)