Enantioselective approach to the asymmetric synthesis of(6R)-hydroxymethyl-5,6-dihydro-2H-pyran-2-one. A formal synthesis of(R)-argentilactone and total synthesis of (R)-goniothalamin

Arkivoc

Volumn 2003, Issue 10, 2003, Pages 118-126

  De Fátima, Ângelo ^a   Pilli, Ronaldo A ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

Catalytic asymmetric Keck allylation and ring closing metathesis; Lemieux Johnson oxidative cleavage; Natural products; Pyranones

Indexed keywords

ARGENTILACTONE; BENZYL ALCOHOL; GONIOTHALAMIN; HYDROXYMETHYL 5,6 DIHYDRO 2H PYRAN 2 ONE; LACTONE DERIVATIVE; NATURAL PRODUCT; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; ASYMMETRIC SYNTHESIS; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOSELECTIVITY; OLEFINATION; PROTON NUCLEAR MAGNETIC RESONANCE; RING CLOSING METATHESIS; WITTIG REACTION;

EID: 0142167849     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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