Unprecedented rearrangement of a 4-alkoxy-5-bromoalk-2-en-1-ol to a cyclopentenone via an iso-nazarov cyclization process

Journal of Organic Chemistry

Volumn 72, Issue 22, 2007, Pages 8565-8568

  Jung, Michael E ^a   Yoo, Dongwon ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACIDIC SUBSTANCE; ALLYLIC ALCOHOL; CYCLOPENTENONE;

ALCOHOLS; CYCLIZATION; REACTION KINETICS;

HYDROCARBONS;

13 DEOXYTEDANOLIDE; ALLYL ALCOHOL; ALUMINUM CHLORIDE; ANTINEOPLASTIC AGENT; BRONSTED ACID; CYCLOPENTENONE; LEWIS ACID; TEDANOLIDE; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; CYCLIZATION; DEBROMINATION; DRUG STRUCTURE; DRUG SYNTHESIS; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; SILYLATION; WITTIG REACTION;

ALKENES; CYCLIZATION; CYCLOPENTANES; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 35549006796     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo071104w     Document Type: Article

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