Total synthesis of (+)-chinensiolide B via tandem allylboration/ lactonization

Journal of the American Chemical Society

Volumn 132, Issue 5, 2010, Pages 1488-1489

  Elford, Tim G ^a   Hall, Dennis G ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

A PLANTS; CARVONE; CHEMICAL EQUATIONS; CHEMO-SELECTIVITY; CHEMOSELECTIVE; ENANTIOSELECTIVE TOTAL SYNTHESIS; FUNCTIONALIZED; LACTONIZATION; LINEAR SEQUENCE; NATURAL PRODUCTS; RING CLOSING METATHESIS; SEVEN-MEMBERED RINGS; STEREO-SELECTIVE; TOTAL SYNTHESIS;

PLANT SHUTDOWNS;

SYNTHESIS (CHEMICAL);

ALLYL COMPOUND; BORANE DERIVATIVE; CHINENSIOLIDE B; GAMMA LACTONE DERIVATIVE; PACLITAXEL; UNCLASSIFIED DRUG;

ARTICLE; BIOLOGICAL ACTIVITY; CATALYSIS; CELL STRAIN HEPG2; CHEMICAL REACTION; CHINESE MEDICINE; CONTROLLED STUDY; CYTOTOXICITY; DRUG ACTIVITY; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; HUMAN; HUMAN CELL; LACTONIZATION; REACTION ANALYSIS; RING CLOSING METATHESIS; STEREOCHEMISTRY;

ASTERACEAE; BIOLOGICAL PRODUCTS; LACTONES; MOLECULAR STRUCTURE; SESQUITERPENES; STEREOISOMERISM;

EID: 76149129379     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9104478     Document Type: Article

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