http://www.cnr.it/ontology/cnr/individuo/prodotto/ID178085
Biocatalytic procedure for obtaining all four diastereoisomers of 1-(1-hydroxyethyl)-3-ethylferrocene: synthons for chiral 1,3-disubstituted ferrocenes. (Articolo in rivista)
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- Biocatalytic procedure for obtaining all four diastereoisomers of 1-(1-hydroxyethyl)-3-ethylferrocene: synthons for chiral 1,3-disubstituted ferrocenes. (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.tetasy.2004.10.032 (literal)
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D'Antona Nicola; Lambusta Daniela; Morrone Raffaele; Nicolosi Giovanni; Secundo Francesco (2004)
Biocatalytic procedure for obtaining all four diastereoisomers of 1-(1-hydroxyethyl)-3-ethylferrocene: synthons for chiral 1,3-disubstituted ferrocenes.
in Tetrahedron: asymmetry (Print); Elsevier Science Ltd., Oxford (Regno Unito)
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- D'Antona Nicola; Lambusta Daniela; Morrone Raffaele; Nicolosi Giovanni; Secundo Francesco (literal)
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- CNR--Istituto di Chimica Biomolecolare Sez. di Catania, Via del Santuario 110, 95028 Valverde CT, Italy; CNR--Istituto di Chimica del Riconoscimento Molecolare, Via Mario Bianco 9, 20131 Milano, Italy (literal)
- Titolo
- Biocatalytic procedure for obtaining all four diastereoisomers of 1-(1-hydroxyethyl)-3-ethylferrocene: synthons for chiral 1,3-disubstituted ferrocenes. (literal)
- Abstract
- Lipase from Candida antarctica has been successfully used to realise the selective esterification of the four 1-(1-hydroxyethyl)-3-ethylferrocene isomers, possessing central/planar chirality. In this reaction, the lipase recognises only the two isomers possessing an (R)-configuration, independently from planar chirality. This allows us to split the mixture into two couples of diastereoisomers, namely the (Sp,Rc)-/(Rp,Rc)- and (Rp,Sc)-/(Sp,Sc)-isomers, conveniently separated in the single constituents by crystallisation from hexane. (literal)
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