A general method for the synthesis of the most powerful naturally occurring Maillard flavors (Articolo in rivista)

Type
Label
  • A general method for the synthesis of the most powerful naturally occurring Maillard flavors (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tet.2007.03.089 (literal)
Alternative label
  • Fuganti C., Gatti F.G., Serra S. (2007)
    A general method for the synthesis of the most powerful naturally occurring Maillard flavors
    in Tetrahedron (Oxf., Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Fuganti C., Gatti F.G., Serra S. (literal)
Pagina inizio
  • 4762 (literal)
Pagina fine
  • 4767 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 63 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • CNR-ICRM Politecnico di Milano (literal)
Titolo
  • A general method for the synthesis of the most powerful naturally occurring Maillard flavors (literal)
Abstract
  • The natural flavors 2-acetyl-1-pyrroline 1a, 2-propionyl-l-pyrroline 1b, 2-acetyl-3,4,5,6-tetrahydropyridine 1c, 2-acetyl-2-thiazoline 1d, 2-propionyl-2-thiazoline 1e, and the artificial flavor 2-acetyl-5,6-dihydro-4H-1,3-thiazine if have been prepared by catalytic SeO2 oxidation of the corresponding cyclic imines 6a-c and sulfur cyclic immes 7a-c using TBHP as co-oxidant. The oxidation of the pyrrolines 1a and b is completely regioselective. Professional olfactory evaluation together with the odor threshold of the new flavor 1f is reported. (literal)
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Autore CNR

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