Large-scale preparation of enantiomerically pure (4aR)-(-)-1,4a-dimethyl-4, 4a,7,8-tetrahydronaphthalene-2,5(3H,6H)-dione: A useful Wieland-Miescher diketone analogue

Synthesis

Volumn , Issue 23, 2008, Pages 3775-3778

  Lanfranchi, Don Antoine ^a   Baldovini, Nicolas ^a   Hanquet, Gilles ^a  

^a CNRS   (France)

Author keywords

Dieckmann condensation; Preferential crystallization; Thiomethylenation; Wieland Miescher diketone

Indexed keywords

OLEFINS;

ASYMMETRIC SYNTHESES; DIECKMANN CONDENSATION; DITERPENES; ENANTIOMERICALLY PURE COMPOUNDS; METHYL CYCLOHEXANES; ONE POTS; PREFERENTIAL CRYSTALLIZATION; PROPIONYL CHLORIDES; SESQUITERPENES; TETRAHYDRO NAPHTHALENES; THIOMETHYLENATION; WIELAND-MIESCHER DIKETONE;

NAPHTHALENE;

1,4A DIMETHYL 4,4A,7,8 TETRAHYDRONAPHTHALENE 2,5(3H,6H)DIONE; 2 METHYLCYCLOHEXANE 1,3 DIONE; DIKETONE; DITERPENE; QUITERPENE; TERPENE DERIVATIVE; UNCLASSIFIED DRUG; WIELAND MIESCHER DIKETONE;

ARTICLE; ASYMMETRIC SYNTHESIS; CYCLIZATION; ENANTIOMER; ONE POT SYNTHESIS;

EID: 57549099394     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0028-1083231     Document Type: Article

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