A synthetic pathway to diquinane and angular triquinane systems via an iron carbonyl promoted tandem [6+2] ene type reaction

Tetrahedron

Volumn 66, Issue 27-28, 2010, Pages 4943-4946

  Pearson, Anthony J ^a   Kim, Eun Hoo ^a   Sun, Huikai ^a  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 ACETYL 5 ETHYL OCTAHYDRO 3 OXO 2 PHENYLCYCLOPENTA[C] PYROLE 3A CARBALDEHYDE; 5 ETHYL 2,3,3A,4,5,5A HEXAHYDRO 2 PHENYLPENTALENO[1 C]PYROLE 1,6 DIONE; 6 METHYL 5 ETHYL 2 PHENYL 2,3,3A,4,5,5A HEXAHYDRO 2 AZACYCLOPENTA[C]INDEN 1 ONE; CARBONYL IRON; DIQUINANE; NATURAL PRODUCT; TRICARBONYL(3 METHYLCYCLOHEXA 1,3 DIENECARBOXYLIC ACID)IRON; TRICARBONYL(6 9 N 6 METHYL 5 ETHYL 2 PHENYL 2,3,3A,4,5,5A HEXAHYDRO 2 AZACYCLO PENTA[C]INDEN 1 ONE)IRON; TRICARBONYL(METHYL 3 METHYLCYCLOHEXA 1,3 DIENECARBOXYLATE)IRON; TRICARBONYL(METHYL 5 METHYLCYCLOHEXA 1,5 DIENECARBOXYLATE)IRON; TRICARBONYL[1 4 N 3 METHYLCYCLOHEXA 1,3 DIENECARBOXYLIC ACID(N PHENYL)HEXA 2,4 DIENYL AMIDE]IRON; TRIQUINANE; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; CROSS COUPLING REACTION; CYCLIZATION; DRUG SYNTHESIS; OZONOLYSIS; PRIORITY JOURNAL;

EID: 77954349244     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.05.018     Document Type: Article

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