FeCl3 catalyzed Prins-type cyclization for the synthesis of highly substituted indenes: Application to the total synthesis of (±)-jungianol and epi-jungianol

Organic Letters

Volumn 15, Issue 3, 2013, Pages 429-431

  Dethe, Dattatraya H ^a   Murhade, Ganesh ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY KANPUR   (India)

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL PRODUCT; CHLORIDE; FERRIC CHLORIDE; FERRIC ION; INDENE DERIVATIVE; JUNGIANOL; SESQUITERPENE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; MEDICINAL PLANT; STEREOISOMERISM; SYNTHESIS;

BIOLOGICAL AGENTS; CATALYSIS; CHLORIDES; CYCLIZATION; FERRIC COMPOUNDS; INDENES; MOLECULAR STRUCTURE; PLANTS, MEDICINAL; SESQUITERPENES; STEREOISOMERISM;

MLCS; MLOWN;

EID: 84873381350     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol3032347     Document Type: Article

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