Photochirogenesis in chiral ionic liquid: Enantiodifferentiating [4+4] photocyclodimerization of 2-anthracenecarboxylic acid in (R)-1-methyl-3-(2,3-dihydroxypropyl)imidazolium bistriflimide (Articolo in rivista)

Type
Label
  • Photochirogenesis in chiral ionic liquid: Enantiodifferentiating [4+4] photocyclodimerization of 2-anthracenecarboxylic acid in (R)-1-methyl-3-(2,3-dihydroxypropyl)imidazolium bistriflimide (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1039/c002448a (literal)
Alternative label
  • Chiappe, Cinzia (1); Mele, Andrea (2); Bellina, Fabio (1); Melai, Bernardo (1); Fukuhara, Gaku (3); Inoue, Yoshihisa (3) (2010)
    Photochirogenesis in chiral ionic liquid: Enantiodifferentiating [4+4] photocyclodimerization of 2-anthracenecarboxylic acid in (R)-1-methyl-3-(2,3-dihydroxypropyl)imidazolium bistriflimide
    in Chemical communications (Lond., 1996, Online); The Royal Society of Chemistry, Cambridge (Regno Unito)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Chiappe, Cinzia (1); Mele, Andrea (2); Bellina, Fabio (1); Melai, Bernardo (1); Fukuhara, Gaku (3); Inoue, Yoshihisa (3) (literal)
Pagina inizio
  • 3472 (literal)
Pagina fine
  • 3474 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 46 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
  • Scopus (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • (1) Dipartimento di Chimica e Chimica Industriale - Università di Pisa; (2) Dipartimento di Chimica - Materiali e Ingegneria Chimica G. Natta; (3) Department of Applied Chemistry - Osaka University (literal)
Titolo
  • Photochirogenesis in chiral ionic liquid: Enantiodifferentiating [4+4] photocyclodimerization of 2-anthracenecarboxylic acid in (R)-1-methyl-3-(2,3-dihydroxypropyl)imidazolium bistriflimide (literal)
Abstract
  • Enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylic acid and its alkali metal salts performed in a chiral ionic liquid gave chiral cyclodimers in good enantiomeric excesses of up to 41%, which is the highest ever reported for a photochirogenic reaction in chiral media. (literal)
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