Advances in the Chemical Synthesis of Medium-sized Cyclitols (Articolo in rivista)

Type
Label
  • Advances in the Chemical Synthesis of Medium-sized Cyclitols (Articolo in rivista) (literal)
Anno
  • 2004-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.2174/1570193043403073 (literal)
Alternative label
  • Rassu, G., Auzzas, L., Battistini, L., Casiraghi, G. (2004)
    Advances in the Chemical Synthesis of Medium-sized Cyclitols
    in Mini-reviews in organic chemistry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Rassu, G., Auzzas, L., Battistini, L., Casiraghi, G. (literal)
Pagina inizio
  • 343 (literal)
Pagina fine
  • 357 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 1 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Battistini, L.; Casiraghi, G. Università degli Studi di Parma, Dipartimento Farmaceutico, Università di Parma, Parco Area delle Scienze 27A, I-43100 Parma, Italy (literal)
Titolo
  • Advances in the Chemical Synthesis of Medium-sized Cyclitols (literal)
Abstract
  • Densely hydroxylated, medium-sized carbocycles and their analogues have long been a somewhat neglected molecular progeny for two reasons: (a) the synthesis of such expanded and functionality rich rings is quite a challenging task that remains partially unsolved and (b) the biological significance of these constructs has not yet been thoroughly appreciated. This account mainly discusses recent approaches used to deal with this rare class of carbohydrate mimics with particular emphasis being placed on annulative strategies using ring-closing metathesis, aldol-based ring closure, intramolecular nitrile oxide and nitrone cycloaddition, and the Claisen rearrangement. Less documented annulative and non-annulative procedures including free-radical cyclisation, intramolecular coupling, and ring expansion and manipulation are also considered. (literal)
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