Enantioselective synthesis and absolute stereochemistry of both the enantiomers of trans-magnolione, a fragrance structurally related to trans-methyl jasmonate

Tetrahedron

Volumn 60, Issue 23, 2004, Pages 4975-4981

  Donnoli, Maria Irene ^a   Scafato, Patrizia ^a   Nardiello, Mariangela ^a   Casarini, Daniele ^a   Giorgio, Egidio ^a   Rosini, Carlo ^a  

^a UNIVERSITY OF BASILICATA   (Italy)

Author keywords

Absolute configuration; Enantioselective Michael addition; Fragrances; Magnolione; Phase transfer catalysis

Indexed keywords

ACETOACETIC ACID; CYCLOPENTENONE; FRAGRANCE; JASMONIC ACID; METHYL GROUP; N METHYLANTHRACENYLQUININIUM; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CIRCULAR DICHROISM; DECARBOXYLATION; ENANTIOMER; ENANTIOSELECTIVITY; HYDROLYSIS; MICHAEL ADDITION; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 2442589745     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.04.038     Document Type: Article

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