Total Synthesis of Terpenoids Employing a "benzannulation of Carvone" Strategy: Synthesis of (-)-Crotogoudin

Journal of the American Chemical Society

Volumn 139, Issue 33, 2017, Pages 11349-11352

  Finkbeiner, Peter ^a   Murai, Kenichi ^b   Röpke, Michael ^a   Sarpong, Richmond ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOADDITION; ETHYLENE; LIPIDS; MONOTERPENES; REGIOSELECTIVITY; SCAFFOLDS;

BICYCLO[2.2.2]OCTANE; DEAROMATIZATION; DIELS-ALDER CYCLOADDITIONS; ENANTIOSPECIFIC SYNTHESIS; ITS APPLICATIONS; NATURAL PRODUCTS; ORGANIC SYNTHESIS; SYNTHETIC APPROACH;

SYNTHESIS (CHEMICAL);

BICYCLO[2.2.2]OCTANE DERIVATIVE; CARBON; CARVONE; DITERPENOID; ETHYLENE; METHYL GROUP; NATURAL PRODUCT; TERPENOID; BIOLOGICAL PRODUCT; CROTOGOUDIN; DITERPENE; ETHYLENE DERIVATIVE; TERPENE; TETRALIN; TETRALIN DERIVATIVE;

AROMATIZATION; ARTICLE; CYCLOADDITION; ENANTIOSELECTIVITY; LACTONIZATION; SYNTHESIS; CHEMISTRY; OXIDATION REDUCTION REACTION; PROCEDURES; STEREOISOMERISM;

BIOLOGICAL PRODUCTS; CYCLOADDITION REACTION; DITERPENES; ETHYLENES; MONOTERPENES; OXIDATION-REDUCTION; STEREOISOMERISM; TETRAHYDRONAPHTHALENES;

EID: 85028082138     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.7b06823     Document Type: Article

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