A stereoselective approach to the azaspiro[5.5]undecane ring system using a conjugate addition/dipolar cycloaddition cascade: Application to the total synthesis of (±)-2,7,8-epi-perhydrohistrionicotoxin

Journal of Organic Chemistry

Volumn 73, Issue 24, 2008, Pages 9601-9609

  Wilson, Michael S ^a   Padwa, Albert ^a  

^a EMORY UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; CONJUGATE ADDITIONS; CUPRATE; CYCLOADDUCT; CYCLOHEXANONE OXIMES; DIASTEREO SELECTIVITIES; DOMINANT FACTORS; HIGH YIELDS; INTRAMOLECULAR DIPOLAR CYCLOADDITION; ISOXAZOLIDINE; NITRONE; ORGANOCUPRATE; OXYGEN BONDS; RING SYSTEMS; STEREOSELECTIVE; TOTAL SYNTHESES; X-RAY CRYSTAL STRUCTURES;

AMIDES; BUTADIENE; CHEMICAL BONDS; CHEMICAL REACTIONS; COPPER COMPOUNDS; CRYSTAL STRUCTURE; CYCLOADDITION; OXYGEN; STEREOCHEMISTRY;

SYNTHESIS (CHEMICAL);

AMPHIBIAN VENOMS; CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 58049204536     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801295e     Document Type: Article

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