Formal synthesis of (-)-anisomycin based on stereoselective nucleophilic substitution along with 1,2-aryl migration

Tetrahedron

Volumn 60, Issue 45, 2004, Pages 10187-10195

  Ono, Machiko ^a   Tanikawa, Shin ^a   Suzuki, Keiko ^a   Akita, Hiroyuki ^a  

^a TOHO UNIVERSITY   (Japan)

Author keywords

( ) Anisomycin; 1,2 Aryl migration; Phenonium ion

Indexed keywords

4 HYDROXY 5 (4' METHOXYPHENYL) 2 PENTENOATE; 5 HYDROXY 4 (4' METHOXYPHENYL) 2 PENTENOATE; ANISOMYCIN; CARBON; CHEMICAL COMPOUND; NITROGEN DERIVATIVE; OSMIUM TETRAOXIDE; SILVER NITRATE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHIRALITY; DRUG SYNTHESIS; HYDROXYLATION; PRIORITY JOURNAL; STEREOCHEMISTRY; SUBSTITUTION REACTION;

EID: 4644227285     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.09.012     Document Type: Article

References (12)

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8. Under this condition, an aryl migration product was not obtained because a catalytic reduction of (±)-13 gave 4-(4′-methoxyphenyl)- pentanoate.
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