Total synthesis and structural revision of the piperarborenines via sequential cyclobutane C-H arylation

Journal of the American Chemical Society

Volumn 133, Issue 47, 2011, Pages 19076-19079

  Gutekunst, Will R ^a   Baran, Phil S ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARYL RINGS; ARYLATIONS; C-H FUNCTIONALIZATION; CYCLOBUTANES; DICARBOXYLATES; DIVERGENT APPROACH; HEAD-TO-HEAD DIMERS; NATURAL PRODUCTS; PHOTOCYCLOADDITION; TOTAL SYNTHESIS;

AROMATIC COMPOUNDS; BUTANE; CARBOXYLATION;

PIPE;

CYCLOBUTANE; NATURAL PRODUCT; PIPERARBORENINE A; PIPERARBORENINE B; PIPERARBORENINE C; PIPERARBORENINE D; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; CANCER CELL; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CROSS COUPLING REACTION; CYCLOADDITION; CYTOTOXICITY; DIMERIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; EPIMERIZATION; HYDROLYSIS; IN VITRO STUDY; ISOMERISM; PHOTOCHEMISTRY; PIPER ARBORESCENS; PIPERACEAE; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; X RAY CRYSTALLOGRAPHY;

CYCLOBUTANES; MOLECULAR STRUCTURE; PIPERIDONES; STEREOISOMERISM;

EID: 81855199815     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja209205x     Document Type: Article

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