http://www.cnr.it/ontology/cnr/individuo/prodotto/ID196233
Study on the stereochemical control of dihydroxylation of vinyl epoxides and their derivatives (Articolo in rivista)
- Type
- Label
- Study on the stereochemical control of dihydroxylation of vinyl epoxides and their derivatives (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.tet.2012.02.029 (literal)
- Alternative label
Righi, Giuliana; Mandic', Emanuela; Naponiello, Gaia Clara Mercedes; Bovicelli, Paolo; Tirotta, Ilaria (2012)
Study on the stereochemical control of dihydroxylation of vinyl epoxides and their derivatives
in Tetrahedron (Oxf., Print); Pergamon-Elsevier Science Ltd., Oxford (Regno Unito)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Righi, Giuliana; Mandic', Emanuela; Naponiello, Gaia Clara Mercedes; Bovicelli, Paolo; Tirotta, Ilaria (literal)
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Univ Roma La Sapienza, Dept Chem, I-00185 Rome, Italy
CNR ICB Unity Rome, I-00185 Rome, Italy
CNR ICB Unity Sassari, I-07040 Sassari, Italy (literal)
- Titolo
- Study on the stereochemical control of dihydroxylation of vinyl epoxides and their derivatives (literal)
- Abstract
- The results obtained from a study on the stereochemical control in the dihydroxylation of the double bond of vinyl epoxides and their derivatives (bromo derivatives, azido derivatives and vinyl aziridines) are presented herein. A significant diastereoselectivity was observed for the bromo derivatives, azido derivatives and N-protected vinyl aziridines, whereas vinyl epoxides and unprotected vinyl aziridines showed no diastereoselectivity. The results obtained are generally consistent with the Kishi model. (C) 2012 Elsevier Ltd. All rights reserved. (literal)
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