http://www.cnr.it/ontology/cnr/individuo/prodotto/ID17661
Stereoselective chemo-enzymatic approaches to the synthesis of C2 1,3-dithiane-1,3-dioxide (Articolo in rivista)
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- Stereoselective chemo-enzymatic approaches to the synthesis of C2 1,3-dithiane-1,3-dioxide (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1080/10426500902856446 (literal)
- Alternative label
Gaggero N., Colonna S., Albanese D., Ottolina G., Del Monte F. (2009)
Stereoselective chemo-enzymatic approaches to the synthesis of C2 1,3-dithiane-1,3-dioxide
in Phosphorus, sulfur, and silicon and the related elements; Gordon and Breach, New York (Stati Uniti d'America)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Gaggero N., Colonna S., Albanese D., Ottolina G., Del Monte F. (literal)
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- http://www.tandfonline.com/doi/abs/10.1080/10426500902856446 (literal)
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- Ist Chim Organ A Marchesini, I-20133 Milan, Italy
Univ Milan, Dipartimento Chim Organ & Ind, Milan, Italy
CNR, Ist Chim Riconoscimento Mol, I-20133 Milan, Italy (literal)
- Titolo
- Stereoselective chemo-enzymatic approaches to the synthesis of C2 1,3-dithiane-1,3-dioxide (literal)
- Abstract
- Two enzyme-mediated methods are presented for the preparation of enantiomerically enriched C 2 1,3-dithiane-1,3-dioxide. The first takes advantage of a trans stereoselective oxidation by NaIO 4 of enantiomerically pure (R) 1,3-dithiane-1-oxide obtained by cyclohexanone monooxygenase. In the second method, a kinetic resolution consisting of a domino hydrolysis-decarboxylation process of (±) 2-carbethoxy-1,3-dithiane-trans-1,3-dioxide is described. The target molecule is obtained with enantiomeric excesses up to 90%. (literal)
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