Regioselective fries rearrangement and friedel-crafts acylation as efficient routes to novel enantiomerically enriched ortho-acylhydroxy[2.2]paracyclophanes

European Journal of Organic Chemistry

Volumn , Issue 19, 2000, Pages 3295-3303

  Rozenberg, Valeria ^a   Danilova, Tat'yana ^a   Sergeeva, Elena ^a   Vorontsov, Evgenii ^a   Starikova, Zoya ^a   Lysenko, Konstantin ^a   Belokon', Yuri ^a  

^a A N NESMEYANOV INSTITUTE OF ORGANOELEMENT COMPOUNDS   (Russian Federation)

Author keywords

Acylations; Asymmetric synthesis; Chiral resolution; Cyclophanes; Fries rearrangement; Lewis acids; Regioselective ortho substitution

Indexed keywords

4 ACETYL 5 HYDROXY[2.2]PARACYCLOPHANE; 4 BENZOYL 5 HYDROXY[2.2]PARACYCLOPHANE; PARACYCLOPHANE DERIVATIVE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHIRALITY; CONFORMATION; ENANTIOMER; REACTION ANALYSIS; X RAY CRYSTALLOGRAPHY;

EID: 0033770481     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200010)2000:19<3295::aid-ejoc3295>3.0.co;2-0     Document Type: Article

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