A novel and concise synthesis of spirodienone alkaloids using hypervalent iodine(III) reagents

Chemical and Pharmaceutical Bulletin

Volumn 52, Issue 10, 2004, Pages 1231-1234

  Hamamoto, Hiromi ^a   Shiozaki, Yukiko ^a   Hata, Kayoko ^a   Tohma, Hirofumi ^a   Kita, Yasuyuki ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

Alkaloid; C C coupling; Heteropoly acid; Hypervalent iodine reagent; Spiro compound

Indexed keywords

3 BENZYLOXY 10,11 DIMETHOXY 7 TRIFLUOACETYL 6,7,7A,8 TETRAHYDRO 5H BIBENZ[D,F]INDOL 2 ONE; 3 BENZYLOXY 6,7 DIMETHOXY 11 TRIFLUOROACETYL 9,10 DIHYDRO 4A,10 PROPANEPHENANTHREN 2 ONE; 3,10,11 TRIMETHOXY 7 PENTAFLUOROBENZOYL 6,7,7A,8 TETRAHYDRO 5H BIBENZ[D,F]INDOL 2 ONE; 6 PENTAFRUOROBENZOYLNORSEBIFERINE; 6 TRIFLUOROACETYLNORSEBIFERINE; ACETONITRILE; ACID; ALKALOID; IODINE; IODINE DERIVATIVE; N TRIFLUOROACETYLNEOSPIRINEDIOENONE; PHENYLIODINE BIS(TRIFLUOROACETATE); REAGENT; SPIRODIENONE ALKALOID DERIVATIVE; TETRAHYDROISOQUINOLINE DERIVATIVE; UNCLASSIFIED DRUG; ACETONITRILE DERIVATIVE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; MORPHINAN DERIVATIVE; SPIRO COMPOUND;

ARTICLE; DRUG SYNTHESIS; INTRAMOLECULAR OXIDATIVE COUPLING; OXIDATION; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; OXIDATION REDUCTION REACTION; SYNTHESIS;

ACETONITRILES; ALKALOIDS; CATALYSIS; INDICATORS AND REAGENTS; MOLECULAR STRUCTURE; MORPHINANS; OXIDATION-REDUCTION; SPIRO COMPOUNDS; TETRAHYDROISOQUINOLINES;

EID: 16644368217     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.52.1231     Document Type: Article

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