A one-pot synthesis of aurones from substituted acetophenones and benzaldehydes: A concise synthesis of aureusidin

Synthesis (Germany)

Volumn 44, Issue 14, 2012, Pages 2217-2224

  Zhao, Xiaolong ^a   Liu, Jie ^a   Xie, Zhixiang ^a   Li, Ying ^a  

^a LANZHOU UNIVERSITY   (China)

Author keywords

bicyclic compounds; cyclizations; furans; heterocycles; natural products; total synthesis

Indexed keywords

BICYCLIC COMPOUNDS; CYCLIZATIONS; FURANS; HETEROCYCLES; NATURAL PRODUCTS; TOTAL SYNTHESIS;

AMORPHOUS ALLOYS; KETONES;

ALDEHYDES;

1 (2 HYDROXY 4,6 DIMETHOXYPHENYL)ETHANONE; 1 (2,4 DICHLORO 6 HYDROXYPHENYL)ETHANONE; 1 [2 (BENZYLOXY) 6 HYDROXYPHENYL]ETHANONE; 1 [2 HYDROXY 4,6 BIS(METHOXYMETHOXY) 3 (3 METHYLBUT 2 EN 1 YL)PHENYL]ETHANONE; 1 [2 HYDROXY 4,6 BIS(METHOXYMETHOXY)PHENYL]ETHANONE; 1 [2 HYDROXY 6 (METHOXYMETHOXY) 4 PYRROLIDIN 1 YLPHENYL]ETHANONE; 1 [2,4 BIS(METHOXYMETHOXY)6 [(3 METHYLBUT 2 EN 1 YL)OXY]PHENYL]ETHANONE; 1 [6 HYDROXY 2,4 BIS(METHOXMETHOXY) 3 (3 METHYLBUT 2 EN 1 YL)PHENYL]ETHANONE; 2 (3,4 DIHYDROXYBENZYLIDENE) 4,6 DIHYDROXY 1 BENZOFURAN 3(2H) ONE; 2 (4 CHLOROBENZYLIDENE) 4,6 DIMETHOXY 1 BENZOFURAN 3(2H) ONE; 2 (4 FLUOROBENZYLIDENE) 4,6 DIMETHOXY 1 BENZOFURAN 3(2H) ONE; 2 (4 METHOXYBENZYLIDENE) 4 (METHOXYMETHOXY) 6 PYRROLIDIN 1 YL 1 BENZOFURAN 3(2H) ONE; 2 (4 METHOXYBENZYLIDENE) 4,6 BIS(METHOXYMETHOXY) 1 BENZOFURAN 3(2H) ONE; 2 [ 3,4 BIS(METHOXYMETHOXY)BENZYLIDENE] 4,6 BIS(METHOXMETHOXY) 1 BENZOFURAN 3(2H) ONE; 3,4 BIS(METHOXYMETHOXY)BENZALDEHYDE; 4 (BENZYLOXY) 2 (4 METHOXYBENZYLIDENE) 1 BENZOFURAN 3(2H) ONE; 4,6 BIS(METHOXYMETHOXY) 2 [4 (METHOXYMETHOXY)BENZYLIDENE] 5 (3 METHYLBUT 2 EN 1 YL) 1 BENZOFURAN 3(2H) ONE; 4,6 BIS(METHOXYMETHOXY) 2 [4 (METHOXYMETHOXY)BENZYLIDENE] 7 (3 METHYLBUT 2 EN 1 YL) 1 BENZOFURAN 3(2H) ONE; 4,6 DICHLORO 2 (4 METHOXYBENZYLIDENE) 1 BENZOFURAN 3(2H) ONE; 4,6 DIMETHOXY 2 (4 METHOXYBENZYLIDENE) 1 BENZOFURAN 3(2H) ONE; ACETOPHENONE DERIVATIVE; BENZALDEHYDE DERIVATIVE; PROTEIN INHIBITOR; THYROXINE DEIODINASE; UNCLASSIFIED DRUG;

ALGAR FLYNN OYAMADA REACTION; ARTICLE; CHEMICAL REACTION; DRUG STRUCTURE; ONE POT SYNTHESIS;

EID: 84863722418     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1291153     Document Type: Article

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