| Disproportionation reaction of disulfides promoted by nitric oxide (NO) in the presence of oxygen. | |
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MedLine Citation:
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PMID: 10465537 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Two disulfides brought about disproportionation reaction to afford an unsymmetrical disulfide in 50% yield with a catalytic amount of nitric oxide in the presence of oxygen. The reaction proceeded faster when alkyl disulfides were employed for the reaction, and the substituent effects suggested that the reaction commenced with an oxidative process. |
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Authors:
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T Itoh; N Tsutsumi; A Ohsawa |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Bioorganic & medicinal chemistry letters Volume: 9 ISSN: 0960-894X ISO Abbreviation: Bioorg. Med. Chem. Lett. Publication Date: 1999 Aug |
Date Detail:
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Created Date: 1999-11-24 Completed Date: 1999-11-24 Revised Date: 2006-11-15 |
Medline Journal Info:
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Nlm Unique ID: 9107377 Medline TA: Bioorg Med Chem Lett Country: ENGLAND |
Other Details:
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Languages: eng Pagination: 2161-6 Citation Subset: IM |
Affiliation:
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School of Pharmaceutical Sciences, Showa University, Tokyo, Japan. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Disulfides
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chemistry* Nitric Oxide / chemistry* Oxygen / chemistry* |
| Chemical | |
Reg. No./Substance:
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0/Disulfides; 10102-43-9/Nitric Oxide; 7782-44-7/Oxygen |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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