C19 quassinoid model studies: Preparation of trans-perhydroindans via a vinylogous Mukaiyama aldol - Free-radical cyclization route

Canadian Journal of Chemistry

Volumn 82, Issue 2, 2004, Pages 314-317

  Donahue, Matthew G ^a   Hart, David J ^a  

^a OHIO STATE UNIVERSITY   (United States)

Author keywords

1,2 asymmetric induction; C19 quassinoids; Free radical cyclization; trans perhydroindans; Vinylogous Mukaiyama aldol reaction

Indexed keywords

ALDEHYDES; FREE RADICALS; KETONES; MATHEMATICAL MODELS; ORGANIC ACIDS; SUBSTRATES; TITANIUM COMPOUNDS;

3,5-DIMETHYLBENZOIC ACID; FREE RADICAL CYCLIZATION; QUASSINOIDS; TITANIUM TETRACHLORIDE;

ALCOHOLS;

3,5 DIMETHYLBENZOIC ACID; ACETAL DERIVATIVE; ALDEHYDE; BENZOIC ACID DERIVATIVE; CARBON; FREE RADICAL; INDAN DERIVATIVE; KETENE DERIVATIVE; TIN DERIVATIVE; TITANIUM TETRACHLORIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CYCLIZATION; MUKAIYAMA REACTION; REACTION ANALYSIS; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 2342524627     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/v03-197     Document Type: Article

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