Concise synthesis of prenylated and geranylated chalcone natural products by regiospecific iodination and Suzuki coupling reactions

Tetrahedron Letters

Volumn 55, Issue 4, 2014, Pages 897-899

  Wang, Haomeng ^a   Yan, Zhihong ^a   Lei, Yanan ^a   Sheng, Kai ^b   Yao, Qingwei ^c   Lu, Kui ^a   Yu, Peng ^a  

^a TIANJIN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b Tianjin Tianfayuan Agency Center for Environmental Protection Affairs Co Ltd   (China)

^c Chemo Dynamics Inc   (United States)

Author keywords

Chalcones; Iodination; Regiospecific; Suzuki coupling reaction

Indexed keywords

2 ,4 ,4 TRIHYDROXY 5 GERANYLCHALCONE; BAVACHALCONE; CHALCONE DERIVATIVE; ISOBAVACHALCONE; ISOXANTHOANGELOL; PRENYLAMINE; UNCLASSIFIED DRUG; XANTHOANGELOL; ALDEHYDE; ALKYL GROUP; NATURAL PRODUCT; PALLADIUM;

ALKYLATION; ARTICLE; CLAISEN REARRANGEMENT; CONTROLLED STUDY; GERANYLATION; IODINATION; PRENYLATION; STEREOCHEMISTRY; SUZUKI REACTION; SYNTHESIS; CATALYST; COLUMN CHROMATOGRAPHY; DRUG SYNTHESIS;

EID: 84892441868     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2013.12.044     Document Type: Article

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