Room-temperature B(OAc) 3-promoted diels-alder reaction of juglone with styrenes: Total syntheses of tetrangulol and anhydrolandomycinone

Journal of Organic Chemistry

Volumn 77, Issue 6, 2012, Pages 2659-2666

  Hsu, Day Shin ^a   Huang, Jiun Yi ^a  

^a NATIONAL CHUNG CHENG UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

2 ,3-DICHLORO-5 ,6-DICYANOBENZOQUINONE; DIELS-ALDER REACTION; GOOD YIELD; JUGLONE; ROOM TEMPERATURE; TOTAL SYNTHESIS;

CHEMICAL REACTIONS;

STYRENE;

ANHYDROLANDOMYCINONE; JUGLONE; LEWIS ACID; QUINONE DERIVATIVE; STYRENE; TETRANGULOL; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLOADDITION; DIELS ALDER REACTION; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; ROOM TEMPERATURE; SYNTHESIS;

BORON COMPOUNDS; CYCLIZATION; MOLECULAR STRUCTURE; NAPHTHOQUINONES; OLIGOSACCHARIDES; STEREOISOMERISM; STYRENES; TEMPERATURE;

EID: 84863349115     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo202448e     Document Type: Article

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