Bidentate Lewis acid catalyzed inverse-electron-demand Diels-Alder reaction for the selective functionalization of aldehydes

Synthesis (Germany)

Volumn 44, Issue 14, 2012, Pages 2195-2199

  Schweighauser, Luca ^a   Bodoky, Ina ^a   Kessler, Simon N ^a   Häussinger, Daniel ^a   Wegner, Hermann A ^a  

^a UNIVERSITY OF BASEL   (Switzerland)

Author keywords

aldehydes; catalysis; Diels Alder reaction; fused ring systems; Lewis acids

Indexed keywords

BIDENTATE LEWIS ACID; DIELS-ALDER; DIELS-ALDER REACTION; ENAMINES; FUSED-RING SYSTEM; IN-SITU; INTRAMOLECULAR DIELS-ALDER REACTION; LEWIS ACID; NATURAL PRODUCTS; PATCHOULI ALCOHOL; REACTION CATALYZED; SELECTIVE FUNCTIONALIZATION; SIDE REACTIONS; TRICYCLIC COMPOUNDS;

ALDEHYDES; FUNCTIONAL GROUPS; NAPHTHALENE; REACTION INTERMEDIATES; SCAFFOLDS;

CATALYSIS;

2 (1 PHENYLETHYL)NAPHTHALENE; 2 (6 METHYLHEPT 5 EN 2 YL)NAPHTHALENE; 2 BENZYLNAPHTHALENE; 2 ISOPROPYLNAPHTHALENE; 2 METHYL 5 [1 (NAPHTHALENE 2 YL)ETHYL]FURAN; 2 METHYL 6 (NAPHTHALENE 2 YL)HEPTAN 2 OL; 2 METHYLNAPHTHALENE; 2 N PROPYLNAPHTHALENE; 2 PENTYLNAPHTHALENE; ALDEHYDE; CITRONELLAL; ENAMINE; ETHYL 2 (NAPHTHALENE 2 YL)PROPANOATE; LEWIS ACID; NAPHTHALENE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; DIELS ALDER REACTION; INVERSE ELECTRON DEMAND DIELS ALDER REACTION;

EID: 84863720700     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1291127     Document Type: Article

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