Synthetic studies on schisandra nortriterpenoids. Stereocontrolled synthesis of enantiopure C-5- epi ABC ring systems of micrandilactone A and lancifodilactone G using RCM

Journal of Organic Chemistry

Volumn 75, Issue 12, 2010, Pages 4192-4200

  Maity, Soumitra ^a   Matcha, Kiran ^a   Ghosh, Subrata ^a  

^a DEPARTMENT OF MATERIALS SCIENCE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEPTENE DERIVATIVES; D-MANNITOL; DI-ENOL; DIHYDROFURANS; ENANTIOPURE; FUNCTIONALIZED; FURO-FURANONE; HYDROBORATION; RING SYSTEMS; SCHISANDRA; STEREOCONTROLLED SYNTHESIS; SYNTHETIC STUDY; UNSATURATED ESTERS;

BROMINE; CLIMATE MODELS; ESTERS; ETHERS; METHANOL; OLEFINS; RUTHENIUM COMPOUNDS;

ENERGY ABSORPTION;

BROMINE; BROMONIUM ION; CYCLOHEPTANE DERIVATIVE; DIHYDROFURAN; ESTER; ETHER DERIVATIVE; FURAN; FURANONE DERIVATIVE; LACTONE; LANCIFODILACTONE G; MANNITOL; METHANOL; MICRANDILACTONE A; NORTRITERPENOID DERIVATIVE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; ETHERIFICATION; NONHUMAN; OXIDATION; SCHISANDRACEAE; STEREOCHEMISTRY;

ANTI-HIV AGENTS; LACTONES; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; RUTHENIUM COMPOUNDS; SCHISANDRA; STEREOISOMERISM; TRITERPENES;

EID: 77953484516     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1006448     Document Type: Article

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