A synthetic entry to the trichothecene nucleus via cargill rearrangement. Formal synthesis of (±)-verrucarol

Synthesis

Volumn , Issue SPEC. ISS. APR., 1998, Pages 619-626

  White, James D ^a   Kim, No Soo ^a   Hill, David E ^a   Thomas, James A ^a  

^a OREGON STATE UNIVERSITY   (United States)

Author keywords

Cargill rearrangement; Trichothecene; Verrucarol; 2+2 photoaddition

Indexed keywords

VERRUCAROL DERIVATIVE;

ARTICLE; CATALYST; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY; CONFORMATIONAL TRANSITION; DRUG CONFORMATION; DRUG SYNTHESIS; STRUCTURE ANALYSIS;

EID: 0031597450     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-5933     Document Type: Article

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