Asymmetric synthesis of (+)-galbelgin, (-)-kadangustin J, (-)-cyclogalgravin and (-)-pycnanthulignenes A and B, three structurally distinct lignan classes, using a common chiral precursor

Journal of Organic Chemistry

Volumn 76, Issue 16, 2011, Pages 6636-6648

  Rye, Claire E ^a   Barker, David ^a  

^a UNIVERSITY OF AUCKLAND   (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE STEREOCHEMISTRY; ARYL RINGS; ASYMMETRIC SYNTHESIS; BENZYLIC; CHIRAL PRECURSORS; ENANTIOSELECTIVE SYNTHESIS; HYDROXYL GROUPS; LIGNANS; MORPHOLINES; PROTECTING GROUP; SUBSTITUTION PATTERNS;

AMIDES; STEREOCHEMISTRY;

CHIRALITY;

CYCLOGALGRAVIN; GALBELGIN; KADANGUSTIN J; LIGNAN DERIVATIVE; PYCNANTHULIGNENES A; PYCNANTHULIGNENES B; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; CHIRALITY; DRUG STRUCTURE; ENANTIOSELECTIVITY;

FURANS; LIGNANS; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 80051727507     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200968f     Document Type: Article

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