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A Useful Application of Benzyl Trichloroacetimidate for the Benzylation of Alcohols

A Useful Application of Benzyl Trichloroacetimidate for the Benzylation of Alcohols

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ECKENBERG, Peter, Ulrich GROTH, Thomas HUHN, Norbert RICHTER, Carsten SCHMECK, 1993. A Useful Application of Benzyl Trichloroacetimidate for the Benzylation of Alcohols. In: Tetrahedron. 49(8), pp. 1619-1624. ISSN 0040-4020. eISSN 1464-5416

@article{Eckenberg1993Usefu-10008, title={A Useful Application of Benzyl Trichloroacetimidate for the Benzylation of Alcohols}, year={1993}, number={8}, volume={49}, issn={0040-4020}, journal={Tetrahedron}, pages={1619--1624}, author={Eckenberg, Peter and Groth, Ulrich and Huhn, Thomas and Richter, Norbert and Schmeck, Carsten} }

<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/10008"> <dc:contributor>Schmeck, Carsten</dc:contributor> <dc:rights>deposit-license</dc:rights> <dc:contributor>Huhn, Thomas</dc:contributor> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T18:15:56Z</dcterms:available> <dc:creator>Eckenberg, Peter</dc:creator> <dc:creator>Richter, Norbert</dc:creator> <dc:contributor>Eckenberg, Peter</dc:contributor> <dcterms:title>A Useful Application of Benzyl Trichloroacetimidate for the Benzylation of Alcohols</dcterms:title> <dcterms:issued>1993</dcterms:issued> <dc:contributor>Richter, Norbert</dc:contributor> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T18:15:56Z</dc:date> <dc:language>eng</dc:language> <dc:format>application/pdf</dc:format> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/10008"/> <dc:creator>Groth, Ulrich</dc:creator> <dc:creator>Huhn, Thomas</dc:creator> <dc:creator>Schmeck, Carsten</dc:creator> <dcterms:rights rdf:resource="https://creativecommons.org/licenses/by-nc-nd/2.0/legalcode"/> <dcterms:abstract xml:lang="eng">Primary, secondary and tertiary alcohols, which are sensitive under basic or acidic reaction conditions, can be 0-benxylated under mild acidic reaction conditions using benxyl 2,2,2-trichloroacetimidate as the benxylation agent. Chiral substrates, which have a tendency towards racemixation under basic reaction conditions, can be benxylated without any loss of chirality.</dcterms:abstract> <dcterms:bibliographicCitation>First publ. in: Tetrahedron 49 (1993), 8, pp. 1619-1624</dcterms:bibliographicCitation> <dc:contributor>Groth, Ulrich</dc:contributor> </rdf:Description> </rdf:RDF>

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