Unambiguous Characterization of the Sesquiterpene (7R,9E)-1,2,11-Trihydroxy-1,3,5,9-bisabolatetraene through Its Enantioselective Synthesis (Articolo in rivista)

Type

• Prodotto della ricerca (Classe)
• Articolo in rivista (Classe)

Label

• Unambiguous Characterization of the Sesquiterpene (7R,9E)-1,2,11-Trihydroxy-1,3,5,9-bisabolatetraene through Its Enantioselective Synthesis (Articolo in rivista) (literal)

Anno

• 2012-01-01T00:00:00+01:00 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi

• 10.1002/ejoc.201200620 (literal)

Alternative label

• Serra, Stefano; Fronza, Giovanni (2012)
  Unambiguous Characterization of the Sesquiterpene (7R,9E)-1,2,11-Trihydroxy-1,3,5,9-bisabolatetraene through Its Enantioselective Synthesis
  in European journal of organic chemistry (Print)
  (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori

• Serra, Stefano; Fronza, Giovanni (literal)

Pagina inizio

• 4838 (literal)

Pagina fine

• 4843 (literal)

Rivista

• European journal of organic chemistry (Rivista)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali

• 6 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo

• 25 (literal)

Note

• ISI Web of Science (WoS) (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni

• Consiglio Nazionale delle Ricerche (CNR) (literal)

Titolo

• Unambiguous Characterization of the Sesquiterpene (7R,9E)-1,2,11-Trihydroxy-1,3,5,9-bisabolatetraene through Its Enantioselective Synthesis (literal)

Abstract

• The bisabolane sesquiterpene (7R,9E)-1,2,11-trihydroxy-1,3,5,9-bisabolatetraene previously extracted from Commiphora kua resins was prepared by enantioselective synthesis using an enzyme-mediated resolution procedure as the key step. Both the chemical structure and the absolute configuration were unambiguously assigned, although the comparison of the obtained analytical data with those previously reported for the isolated terpene indicated a possible error in the characterization of the natural product. A further study on the chemical stability of the aforementioned compound revealed that it is very unstable in an acidic environment, where it cyclizes readily to give the corresponding chromane derivatives. (literal)

Prodotto di

• Applicazioni sintetiche della biocatalisi (PM.P03.009.002) (Modulo)
• Istituto di chimica del riconoscimento molecolare (ICRM) (Istituto)

Autore CNR

• GIOVANNI FRONZA (Unità di personale esterno)
• STEFANO SERRA (Unità di personale interno)

Insieme di parole chiave

• Parole chiave di "Unambiguous Characterization of the Sesquiterpene (7R,9E)-1,2,11-Trihydroxy-1,3,5,9-bisabolatetraene through Its Enantioselective Synthesis" (Insieme di parole chiave)

Incoming links:

Autore CNR di

• STEFANO SERRA (Unità di personale interno)
• GIOVANNI FRONZA (Unità di personale esterno)

Prodotto

• Istituto di chimica del riconoscimento molecolare (ICRM) (Istituto)
• Applicazioni sintetiche della biocatalisi (PM.P03.009.002) (Modulo)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi

• European journal of organic chemistry (Rivista)

Insieme di parole chiave di

• Parole chiave di "Unambiguous Characterization of the Sesquiterpene (7R,9E)-1,2,11-Trihydroxy-1,3,5,9-bisabolatetraene through Its Enantioselective Synthesis" (Insieme di parole chiave)