File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Lewis Acid Promoted Phenylseleno Group Transfer Tandem Radical Cyclization Reactions

TitleLewis Acid Promoted Phenylseleno Group Transfer Tandem Radical Cyclization Reactions
Authors
Issue Date2002
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html
Citation
Organic Letters, 2002, v. 4 n. 7, p. 1239-1241 How to Cite?
Abstractmatrix presented A new Lewis acid promoted phenylseleno group transfer tandem radical cyclization method was developed. In the presence of Lewis acids such as Yb(OTf) 3 or Mg(Cl0 4) 2, under photolysis condition at low temperature (-45°C), various unsaturated α-phenylseleno β-keto amides underwent radical cyclization reactions to give monocyclic or bicyclic products in a highly efficient, regioselective, and stereoselective manner.
Persistent Identifierhttp://hdl.handle.net/10722/69213
ISSN
2015 Impact Factor: 6.732
2015 SCImago Journal Rankings: 3.187
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorYang, Den_HK
dc.contributor.authorGao, Qen_HK
dc.contributor.authorLee, OYen_HK
dc.date.accessioned2010-09-06T06:11:36Z-
dc.date.available2010-09-06T06:11:36Z-
dc.date.issued2002en_HK
dc.identifier.citationOrganic Letters, 2002, v. 4 n. 7, p. 1239-1241en_HK
dc.identifier.issn1523-7060en_HK
dc.identifier.urihttp://hdl.handle.net/10722/69213-
dc.description.abstractmatrix presented A new Lewis acid promoted phenylseleno group transfer tandem radical cyclization method was developed. In the presence of Lewis acids such as Yb(OTf) 3 or Mg(Cl0 4) 2, under photolysis condition at low temperature (-45°C), various unsaturated α-phenylseleno β-keto amides underwent radical cyclization reactions to give monocyclic or bicyclic products in a highly efficient, regioselective, and stereoselective manner.en_HK
dc.languageengen_HK
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.htmlen_HK
dc.relation.ispartofOrganic Lettersen_HK
dc.titleLewis Acid Promoted Phenylseleno Group Transfer Tandem Radical Cyclization Reactionsen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1523-7060&volume=4&issue=7&spage=1239&epage=1241&date=2002&atitle=Lewis+acid+promoted+phenylseleno+group+transfer+tandem+radical+cyclization+reactionsen_HK
dc.identifier.emailYang, D:yangdan@hku.hken_HK
dc.identifier.emailLee, OY:leeonyi@hku.hken_HK
dc.identifier.authorityYang, D=rp00825en_HK
dc.identifier.authorityLee, OY=rp00725en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ol025750nen_HK
dc.identifier.pmid11922828-
dc.identifier.scopuseid_2-s2.0-0042375996en_HK
dc.identifier.hkuros68458en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0042375996&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume4en_HK
dc.identifier.issue7en_HK
dc.identifier.spage1239en_HK
dc.identifier.epage1241en_HK
dc.identifier.isiWOS:000174680100049-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridYang, D=7404800756en_HK
dc.identifier.scopusauthoridGao, Q=7202743913en_HK
dc.identifier.scopusauthoridLee, OY=7103020334en_HK

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats