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Construction of Bi- and tricyclic skeletons by domino-Heck-Diels-Alder reactions

Title: Construction of Bi- and tricyclic skeletons by domino-Heck-Diels-Alder reactions
Authors: Korbe, S.; de Meijere, Armin; Labahn, T.
Contributors: Korbe, S.; de Meijere, Armin; Labahn, T.
Publisher Information: Wiley-v C H Verlag Gmbh
Publication Year: 2002
Collection: Georg-August-Universität Göttingen: GoeScholar
Description: Palladium-catalyzed intramolecular reactions of 2-bromo 1,6-dienes followed by intermolecular [4+2] cycloaddition with suitable dienophiles in one-pot operations gave hexahydroindenes 8 and 9 in yields of 40-78%, an hexahydro-s-indacene derivative 13 could be obtained in up to 25% yield with cyclopent-2-en-1-one (10) as a dienophile in the presence of different Lewis acids, and a spirocyclopentane-hexahydroindenone 18 could be isolated in 72% yield. When in-situ-formed iminium salts were used as heterodienophiles, hexahydro-1H-[2]pyrindinols 31 could be obtained in a one-pot two-step operation in 29-46% yield.
Document Type: article in journal/newspaper
Language: unknown
Relation: 000179216100011
Availability: https://resolver.sub.uni-goettingen.de/purl?gro-2/44539
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.1053ED4B
Database: BASE