Revision and confirmation of the regiochemistry of isoxazoles derived from methyl oleanonate and lanost-8-en-3-one. Synthesis of a new lanostane triterpenoid with a cyano-enone functionality in ring A

Journal of Organic Chemistry

Volumn 68, Issue 12, 2003, Pages 4991-4993

  Honda, Yukiko ^a   Honda, Tadashi ^a   Roy, Sujata ^a   Gribble, Gordon W ^a  

^a Dartmouth College   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

REGIOCHEMISTRY;

BIOCHEMICAL ENGINEERING; ESTERS; SYNTHESIS (CHEMICAL);

KETONES;

2 (HYDROXYMETHYLENE)LANOST 8 EN 3 ONE; 3 OXALANOSTA 1,8 DIENE 2 CARBONITRILE; [2,3 D]ISOXAZOLE; ISOXAZOLE DERIVATIVE; LANOST 8 EN 3 ONE; LANOST 8 ENO[2,3 D]ISOXAZOLE; LANOSTANE; METHYL OLEANONATE; METHYLISOXAZOLO[4,5 B]OLEAN 12 EN 28 OATE; NATURAL PRODUCT; TRITERPENE; TRITERPENOID; UNCLASSIFIED DRUG;

ANTIINFLAMMATORY ACTIVITY; ANTINEOPLASTIC ACTIVITY; ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STRUCTURE ANALYSIS;

CYCLIZATION; ISOXAZOLES; LANOSTEROL; MOLECULAR STRUCTURE; OLEANOLIC ACID; STEREOISOMERISM; TRITERPENES;

EID: 0037601992     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo034056y     Document Type: Article

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