Palladium-catalyzed routes to geranylated or farnesylated phenolic stilbenes: Synthesis of pawhuskin C and schweinfurthin J

Synthesis (Germany)

Volumn 44, Issue 18, 2012, Pages 2895-2902

  Singh, Mandeep ^a   Argade, Narshinha P ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

geranylated or farnesylated stilbenes; natural products; palladium catalyzed coupling reactions; phloroglucinol; total synthesis

Indexed keywords

COUPLING REACTION; GERANYLATED OR FARNESYLATED STILBENES; NATURAL PRODUCTS; PHLOROGLUCINOL; TOTAL SYNTHESIS;

ACETYLENE; CATALYSIS; STEREOSELECTIVITY;

PHENOLS;

1 (2 IODOVINYL) 4 (METHOXYMETHOXY)BENZENE; 1 (METHOXYMETHOXY) 4 VINYLBENZENE; 1 [(3,7 DIMETHYLOCTA 2,6 DIENYL)OXY] 3,5 BIS(METHOXYMETHOXY)BENZENE; 1 ETHYNYL 4 (METHOXYMETHOXY)BENZENE; 1,2 BIS(METHOXYMETHOXY) 4 VINYLBENZENE; 1,3 BIS(METHOXYMETHOXY) 5 [( 3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)OXY]BENZENE; 1,3 BIS(METHOXYMETHOXY) 5 [4 (METHOXYMETHOXY)STYRYL] 2 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)BENZENE; 1,3 BIS(METHOXYMETHOXY) 5 [[4 (METHOXYMETHOXY)PHENYL]ETHYNYL] 2 ( 3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)BENZENE; 2 [3,4 BIS(METHOXYMETHOXY)STYRYL] 4,4,5,5 TETRAMETHYL 1,3,2 DIOXABOROLANE; 2 [4 (METHOXYMETHOXY)STYRYL] 4,4,5,5 TETRAMETHYL 1,3,2 DIOXABOROLANE; 3,5 BIS(METHOXYMETHOXY) 4 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)PHENOL; 3,5 BIS(METHOXYMETHOXY) 4 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)PHENYL TRIFLUOROMETHANESULFONATE; 4 (2 IODOVINYL) 1,2 BIS(METHOXYMETHOXY)BENZENE; 4 (3,7 DIMETHYLOCTA 2,6 DIENYL) 3,5 BIS(METHOXYMETHOXY)PHENOL; 4 (3,7 DIMETHYLOCTA 2,6 DIENYL) 3,5 BIS(METHOXYMETHOXY)PHENYL TRIFLUOROMETHANESULFONATE; 4 [4 (3,7 DIMETHYLOCTA 2,6 DIENYL) 3,5 DIHYDROXYSTYRYL]BENZENE 1,2 DIOL; 5 (4 HYDROXYSTYRYL) 2 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)BENZENE 1,3 DIOL; 5 [ 3,4 BIS(METHOXYMETHOXY)STYRYL] 2 (3,7 DIMETHYLOCTA 2,6 DIENYL) 1,3 BIS(METHOXYMETHOXY)BENZENE; NATURAL PRODUCT; PALLADIUM; PAWHUSKIN C; PHENOL DERIVATIVE; SCHWEINFURTHIN J; STILBENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL INTERACTION; DRUG STRUCTURE; DRUG SYNTHESIS; ISOMERIZATION; SONOGASHIRA REACTION; STEREOCHEMISTRY;

EID: 84866081662     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0032-1316765     Document Type: Article

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