Total synthesis of (± )-trans-dihydronarciclasine through a highly endo-selective Diels-Alder cycloaddition of 3,5-dibromo-2-pyrone

Angewandte Chemie - International Edition

Volumn 46, Issue 13, 2007, Pages 2303-2305

  Shin, In Ji ^a   Choi, Eun Sil ^a   Cho, Cheon Gyu ^a  

^a Hanyang University   (South Korea)

Author keywords

Antitumor agents; Cycloaddition; Lactones; Natural products; Total synthesis

Indexed keywords

BINDING ENERGY; CYCLOADDITION; STYRENE; SYNTHESIS (CHEMICAL);

3,5-DIBROMO-2-PYRONE; LACTONES; NATURAL PRODUCTS;

CHEMICAL COMPOUNDS;

3,5 DIBROMO 2 PYRONE; 3,5-DIBROMO-2-PYRONE; ALKALOID; DIHYDRONARCICLASINE; HERBACEOUS AGENT; PLANT EXTRACT; PYRONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; HUMAN; SYNTHESIS;

ALKALOIDS; DRUGS, CHINESE HERBAL; HUMANS; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; PLANT EXTRACTS; PYRONES;

EID: 34250323132     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200604612     Document Type: Article

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