A nucleophile-catalyzed cycloisomerization permits a concise synthesis of (+)-harziphilone

Proceedings of the National Academy of Sciences of the United States of America

Volumn 101, Issue 33, 2004, Pages 12064-12066

  Stark, Lucy M ^a   Pekari, Klaus ^a   Sorensen, Erik J ^a,b  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b PRINCETON UNIVERSITY   (United States)

Author keywords

Baylis Hillman reaction; Conjugate additions; Domino reactions; Electrocyclizations; Nucleophilic catalysis

Indexed keywords

DIKETONE; HARZIPHILONE; REV PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; BAYLIS HILLMAN REACTION; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; DNA RESPONSIVE ELEMENT; HUMAN IMMUNODEFICIENCY VIRUS 1; ISOMERIZATION; PRIORITY JOURNAL; REV RESPONSIVE ELEMENT; SYNTHESIS;

ANTI-HIV AGENTS; BENZOPYRANS; CATALYSIS; CHEMISTRY, ORGANIC; MOLECULAR STRUCTURE; PIPERAZINES; STEREOISOMERISM;

HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 4344625385     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0402563101     Document Type: Article

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