Syntheses of (-)-cryptocaryolone and (-)-cryptocaryolone diacetate via a diastereoselective oxy-Michael addition and oxocarbenium allylation

Journal of Organic Chemistry

Volumn 77, Issue 16, 2012, Pages 6929-6936

  Albury, Aymara M M ^a   Jennings, Michael P ^a  

^a UNIVERSITY OF ALABAMA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL FORMATION; BRIDGED STRUCTURES; DIASTEREOSELECTIVE; HOMOALLYLIC ALCOHOL; LINEAR PORTIONS; OXOCARBENIUM; OXY-MICHAEL ADDITIONS; TOTAL SYNTHESIS; WACKER OXIDATION;

ADDITION REACTIONS; ALLYLATION; SUGARS;

STEREOSELECTIVITY;

CARBON; CRYPTOCARYOLONE; CRYPTOCARYOLONE DIACETATE; GLYCOSIDE; OXOCARBENIUM; OXYGEN DERIVATIVE; PLANT EXTRACT; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; MICHAEL ADDITION; OXY MICHAEL ADDITION; STEREOCHEMISTRY;

ACETALS; ALCOHOLS; CATALYSIS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; MONOSACCHARIDES; OXIDATION-REDUCTION; PYRONES; STEREOISOMERISM;

EID: 84865230588     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo301122b     Document Type: Article

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