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Article: Organosilanes in copper-mediated conjugate reductions and reductive aldol reactions

TitleOrganosilanes in copper-mediated conjugate reductions and reductive aldol reactions
Authors
Chiu, P
KeywordsAldol reactions
Copper conjugate reductions
Organosilanes
Issue Date2004
PublisherGeorg Thieme Verlag. The Journal's web site is located at www.thieme-chemistry.com
Citation
Synthesis, 2004 n. 13, p. 2210-2215 How to Cite?
DOI: http://dx.doi.org/10.1055/s-2004-831172
AbstractOrganosilanes have been used to synthesize and regenerate copper hydrides, and have been employed as stoichiometric reductants in the copper-catalyzed reductions of a variety of activated olefins. Reductive aldol condensations and cyclizations using organosilanes and transition metal catalysts, including copper hydrides, have also been achieved.
Persistent Identifierhttp://hdl.handle.net/10722/70234
ISSN
0039-7881
2023 Impact Factor: 2.2
2023 SCImago Journal Rankings: 0.582
ISI Accession Number ID
WOS:000223845000020
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorChiu, Pen_HK
dc.date.accessioned2010-09-06T06:20:58Z-
dc.date.available2010-09-06T06:20:58Z-
dc.date.issued2004en_HK
dc.identifier.citationSynthesis, 2004 n. 13, p. 2210-2215en_HK
dc.identifier.issn0039-7881en_HK
dc.identifier.urihttp://hdl.handle.net/10722/70234-
dc.description.abstractOrganosilanes have been used to synthesize and regenerate copper hydrides, and have been employed as stoichiometric reductants in the copper-catalyzed reductions of a variety of activated olefins. Reductive aldol condensations and cyclizations using organosilanes and transition metal catalysts, including copper hydrides, have also been achieved.en_HK
dc.languageengen_HK
dc.publisherGeorg Thieme Verlag. The Journal's web site is located at www.thieme-chemistry.comen_HK
dc.relation.ispartofSynthesisen_HK
dc.subjectAldol reactionsen_HK
dc.subjectCopper conjugate reductionsen_HK
dc.subjectOrganosilanesen_HK
dc.titleOrganosilanes in copper-mediated conjugate reductions and reductive aldol reactionsen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0039-7857&volume=&spage=2210&epage=2215&date=2004&atitle=Organosilanes+in+copper-mediated+conjugate+reductions+and+reductive+aldol+reactionsen_HK
dc.identifier.emailChiu, P:pchiu@hku.hken_HK
dc.identifier.authorityChiu, P=rp00680en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1055/s-2004-831172en_HK
dc.identifier.scopuseid_2-s2.0-4544221000en_HK
dc.identifier.hkuros98599en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-4544221000&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.issue13en_HK
dc.identifier.spage2210en_HK
dc.identifier.epage2215en_HK
dc.identifier.isiWOS:000223845000020-
dc.publisher.placeGermanyen_HK
dc.identifier.scopusauthoridChiu, P=11140148700en_HK
dc.identifier.issnl0039-7881-

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