Singlet oxygen addition to chiral allylic alcohols and subsequent peroxyacetalization with β-naphthaldehyde: synthesis of diastereomerically pure 3-β-naphthyl-substituted 1,2,4-trioxanes

Tetrahedron

Volumn 62, Issue 46, 2006, Pages 10615-10622

  Griesbeck, Axel G ^a   El Idreesy, Tamer T ^a   Lex, Johann ^a  

^a UNIVERSITY OF COLOGNE   (Germany)

Author keywords

1,2,4 Trioxanes; Catalysis; Ene reaction; Peroxyacetalization; Singlet oxygen

Indexed keywords

3 (NAPHTHALEN 2 YL) 6 (PROP 1 EN 2 YL) 5 PROPYL 1,2,4 TRIOXANE; 3,5 DICYCLOHEXYL 6 (PROP 1 EN 2 YL) 1,2,4 TRIOXANE; 5 ALLYL 3 (NAPHTHALEN 2 YL) 6 (PROP 1 EN 2 YL) 1,2,4 TRIOXANE; 5 BUTYL 3 (NAPHTHALEN 2 YL) 6 (PROP 1 EN 2 YL) 1,2,4 TRIOXANE; 5 CYCLOHEXYL 3 (NAPHTHALEN 2 YL) 6 (PROP 1 EN 2 YL) 1,2,4 TRIOXANE; 5 CYCLOPROPYL 3 (NAPHTHALEN 2 YL) 6 (PROP 1 EN 2 YL) 1,2,4 TRIOXANE; 5 ETHYL 3 (NAPHTHALEN 2 YL) 6 (PROP 1 EN 2 YL) 1,2,4 TRIOXANE; 5 ISOBUTYL 3 (NAPHTHALEN 2 YL) 6 (PROP 1 EN 2 YL) 1,2,4 TRIOXANE; ALCOHOL; ALDEHYDE; BUT 3 EN 2 YL 3 (NAPHTHALEN 2 YL) 6 (PROP 1 EN 2 YL) 1,2,4 TRIOXANE; NAPHTHALENE DERIVATIVE; SINGLET OXYGEN; UNCLASSIFIED DRUG;

ACETALIZATION; ARTICLE; CATALYSIS; CHIRALITY; CROSS LINKING; CRYSTAL STRUCTURE; DIASTEREOISOMER; DRUG SYNTHESIS; PHOTOOXIDATION; PRIORITY JOURNAL; SOLID STATE; SUBSTITUTION REACTION;

EID: 33749343243     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.05.093     Document Type: Article

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