http://www.cnr.it/ontology/cnr/individuo/prodotto/ID16735
Pyrrolizidine Alkaloids via Intramolecular Palladium-Catalysed Allylic Alkylation: Synthesis of (+-)-Isoretronecanol (Articolo in rivista)
- Type
- Label
- Pyrrolizidine Alkaloids via Intramolecular Palladium-Catalysed Allylic Alkylation: Synthesis of (+-)-Isoretronecanol (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/ejoc.200400135 (literal)
- Alternative label
Sebastien, Lemaire; Giuliano, Giambastiani; Guillaume, Prestat; Giovanni, Poli (2004)
Pyrrolizidine Alkaloids via Intramolecular Palladium-Catalysed Allylic Alkylation: Synthesis of (+-)-Isoretronecanol
in European journal of organic chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Sebastien, Lemaire; Giuliano, Giambastiani; Guillaume, Prestat; Giovanni, Poli (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Institute of Chemistry of OrganoMetallic Compounds, ICCOM-CNR, Florence research area, Via Madonna del Piano 10 - 50019 - Sesto Fiorentino - Florence - Italy; Laboratoire de Chimie Organique, UMR 7611 CNRS, Universite Pierre et Marie Curie, 4, Place Jussieu Bo?te 183, 75252, Paris, France (literal)
- Titolo
- Pyrrolizidine Alkaloids via Intramolecular Palladium-Catalysed Allylic Alkylation: Synthesis of (+-)-Isoretronecanol (literal)
- Abstract
- An efficient and stereoconvergent approach to 3-substituted hexahydroindol-2-one derivatives by palladium-catalysed intramolecular allylic alkylation has been developed. Subsequently, the straightforward conversion of the hexahydroindol-2-one 7d into the alkaloid (±)-isoretronecanol has been performed. The synthesis entails 11 steps starting from 1,3-cyclohexadiene, affording the final target in a 29% overall yield. (literal)
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