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- Publisher Website: 10.1021/ol100587j
- Scopus: eid_2-s2.0-77951790038
- PMID: 20387852
- WOS: WOS:000277212800054
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Article: Mild arming and derivatization of natural products via an In(OTf) 3-catalyzed arene iodination
Title | Mild arming and derivatization of natural products via an In(OTf) 3-catalyzed arene iodination |
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Authors | |
Issue Date | 2010 |
Publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html |
Citation | Organic Letters, 2010, v. 12 n. 9, p. 2104-2107 How to Cite? |
Abstract | Figure presented Iodination of arene-containing natural products employing N-iodosuccinimide catalyzed by In(OTf)3 at ambient temperature is reported as a versatile and mild method for natural product derivatization amenable to small scale. This process facilitates natural product derivatization of arene moieties for SAR studies, homo- and heterodimerization of natural products, and also conjugation with reporters such as biotin via subsequent metal-mediated coupling reactions. © 2010 American Chemical Society. |
Persistent Identifier | http://hdl.handle.net/10722/168452 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.245 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Zhou, CY | en_US |
dc.contributor.author | Li, J | en_US |
dc.contributor.author | Peddibhotla, S | en_US |
dc.contributor.author | Romo, D | en_US |
dc.date.accessioned | 2012-10-08T03:19:05Z | - |
dc.date.available | 2012-10-08T03:19:05Z | - |
dc.date.issued | 2010 | en_US |
dc.identifier.citation | Organic Letters, 2010, v. 12 n. 9, p. 2104-2107 | en_US |
dc.identifier.issn | 1523-7060 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/168452 | - |
dc.description.abstract | Figure presented Iodination of arene-containing natural products employing N-iodosuccinimide catalyzed by In(OTf)3 at ambient temperature is reported as a versatile and mild method for natural product derivatization amenable to small scale. This process facilitates natural product derivatization of arene moieties for SAR studies, homo- and heterodimerization of natural products, and also conjugation with reporters such as biotin via subsequent metal-mediated coupling reactions. © 2010 American Chemical Society. | en_US |
dc.language | eng | en_US |
dc.publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html | en_US |
dc.relation.ispartof | Organic Letters | en_US |
dc.subject.mesh | Biological Agents - Chemistry | en_US |
dc.subject.mesh | Catalysis | en_US |
dc.subject.mesh | Indium - Chemistry | en_US |
dc.subject.mesh | Structure-Activity Relationship | en_US |
dc.subject.mesh | Succinimides - Chemistry | en_US |
dc.subject.mesh | Temperature | en_US |
dc.title | Mild arming and derivatization of natural products via an In(OTf) 3-catalyzed arene iodination | en_US |
dc.type | Article | en_US |
dc.identifier.email | Zhou, CY:cyzhou@hku.hk | en_US |
dc.identifier.authority | Zhou, CY=rp00843 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1021/ol100587j | en_US |
dc.identifier.pmid | 20387852 | - |
dc.identifier.scopus | eid_2-s2.0-77951790038 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77951790038&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 12 | en_US |
dc.identifier.issue | 9 | en_US |
dc.identifier.spage | 2104 | en_US |
dc.identifier.epage | 2107 | en_US |
dc.identifier.isi | WOS:000277212800054 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Zhou, CY=35742480200 | en_US |
dc.identifier.scopusauthorid | Li, J=36078695800 | en_US |
dc.identifier.scopusauthorid | Peddibhotla, S=8763117300 | en_US |
dc.identifier.scopusauthorid | Romo, D=7004023555 | en_US |
dc.identifier.issnl | 1523-7052 | - |