Concise synthesis of licochalcone a through water-accelerated [3,3]-sigmatropic rearrangement of an aryl prenyl ether

Synthesis

Volumn , Issue 3, 2011, Pages 370-376

  Jeon, Jae Ho ^a   Kim, Mi Ran ^a   Jun, Jong Gab ^a  

^a Hallym University   (South Korea)

Author keywords

condensation; licochalcone A; natural products; rearrangements

Indexed keywords

ACETOPHENONES; ALLYL ARYL ETHERS; AQUEOUS ETHANOL; BIOLOGICAL ACTIVITIES; CHALCONES; CLAISEN REARRANGEMENT; CLAISEN SCHMIDT CONDENSATION; CONCISE SYNTHESIS; GOOD YIELD; LICOCHALCONE A; METHOXY; MILD ACIDIC CONDITIONS; NATURAL PRODUCTS; REARRANGEMENTS; SEALED TUBES; SIGMATROPIC REARRANGEMENT REACTION; SIGMATROPIC REARRANGEMENTS; TETRAHYDROPYRAN;

ALDEHYDES; CONDENSATION; ETHANOL; KETONES; MICROWAVE IRRADIATION; SYNTHESIS (CHEMICAL);

ETHERS;

2 METHOXY 4 [(3 METHYLBUT 2 EN 1 YL)OXY]BENZALDEHYDE; 4 (TETRAHYDROPYRAN 2 YLOXY)ACETOPHENONE; ACETOPHENONE DERIVATIVE; ALCOHOL; ALLYL ARYL ETHER; ARYL PRENYL ETHER; BENZALDEHYDE DERIVATIVE; ETHER DERIVATIVE; LICOCHALCONE A; UNCLASSIFIED DRUG; WATER;

ARTICLE; CLAISEN REARRANGEMENT; CONTROLLED STUDY; HEATING; MICROWAVE IRRADIATION; PRENYLATION; REACTION OPTIMIZATION;

EID: 79151480340     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1258381     Document Type: Article

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