http://www.cnr.it/ontology/cnr/individuo/prodotto/ID255674
Desymmetrization of cis-1,2-dihydroxycycloalkanes by stereoselective lipase mediated esterification (Articolo in rivista)
- Type
- Label
- Desymmetrization of cis-1,2-dihydroxycycloalkanes by stereoselective lipase mediated esterification (Articolo in rivista) (literal)
- Anno
- 1995-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/0957-4166(95)00035-N (literal)
- Alternative label
Giovanni Nicolosi, Angela Patti, Mario Piattelli, Claudia Sanfilippo (1995)
Desymmetrization of cis-1,2-dihydroxycycloalkanes by stereoselective lipase mediated esterification
in Tetrahedron: asymmetry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Giovanni Nicolosi, Angela Patti, Mario Piattelli, Claudia Sanfilippo (literal)
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- http://dx.doi.org/10.1016/0957-4166(95)00035-N (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto del CNR per lo Studio delle Sostanze Naturali di Interesse Alimentare e Chimico-farmaceutico (literal)
- Titolo
- Desymmetrization of cis-1,2-dihydroxycycloalkanes by stereoselective lipase mediated esterification (literal)
- Abstract
- Meso-compounds 1,2-dihydroxycyclopentane (1), 1,2-dihydroxycyclohexane (2) and 1,2-dyhydroxycycloheptane (3) were desymmetrised by enantiotoposelective esterification with vinyl acetate in tert-butyl methyl ether catalysed by lipases from Pseudomonas cepacia, Candida antarctica (Novozym 435®) and Mucor miehei (Lipozyme TM®). Both of the lipases from P. cepacia and M. miehei afforded the (1S,2R)-acetate (+)-1a and (1R,2S)-acetates (-)-2a and (+)-3a in good enantiomeric excesses and chemical yield. (literal)
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- Autore CNR
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