http://www.cnr.it/ontology/cnr/individuo/prodotto/ID15793
Chemoenzymatic access to all four enantiopure stereoisomers of 1-ferrocenyl-1,3-butanediol (Articolo in rivista)
- Type
- Label
- Chemoenzymatic access to all four enantiopure stereoisomers of 1-ferrocenyl-1,3-butanediol (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.tetasy.2006.01.028 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Patti A.; Pedotti S. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://www.sciencedirect.com/science/article/pii/S0957416606000711 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- Scopu (literal)
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto di Chimica Biomolecolare Sez. di Catania, Via del Santuario 110, I-95028 Valverde CT, Italy (literal)
- Titolo
- Chemoenzymatic access to all four enantiopure stereoisomers of 1-ferrocenyl-1,3-butanediol (literal)
- Abstract
- The kinetic resolution of ferrocenyl aldol 2 was achieved by a lipase-catalyzed esterification in organic solvent. Lipase from Candida antarctica was also found effective in promoting the enantioselective alcoholysis of acetate (±)-3 with n-BuOH. Both enantiomers of 2 were obtained in enantiopure form and subjected to chemical reduction to afford the corresponding syn- and anti-diols. These diols serve as starting materials for the preparation of new ferrocenyl amino alcohols bearing two stereocenters in the side chain. (literal)
- Prodotto di
- Autore CNR
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