Enantiopure 2,2′-dihydroxy-3,3′-dimethoxy-5,5′-diallyl-6, 6′-dibromo-1,1′-biphenyl: A conformationally stable C 2-dimer of a eugenol derivative

Tetrahedron Asymmetry

Volumn 15, Issue 2, 2004, Pages 275-282

  Delogu, Giovanna ^a   Fabbri, Davide ^a   Dettori, Maria Antonietta ^a   Forni, Alessandra ^b   Casalone, Gianluigi ^b  

^a CNR   (Italy)

^b CNR Consiglio Nazionale delle Ricerche   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

2,2' DIHYDROXY 3,3' DIMETHOXY 5,5' DIALLYL 6,6' DIBROMO 1,1' BIPHENYL; BIPHENYL DERIVATIVE; CARBONIC ACID DERIVATIVE; DIMER; EUGENOL; PHOSPHOROTHIOAMIDATE; PHOSPHORUS DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CORRELATION ANALYSIS; CRYSTAL STRUCTURE; DIASTEREOISOMER; DRUG CONFORMATION; DRUG SYNTHESIS; ENANTIOSELECTIVITY; MOLECULAR STABILITY; PRIORITY JOURNAL; QUANTUM YIELD; REACTION ANALYSIS; REDUCTION; STRUCTURE ANALYSIS; X RAY ANALYSIS;

EID: 0347600475     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2003.11.020     Document Type: Article

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