A general approach to the asymmetric synthesis of lignans: (-)-methyl piperitol, (-)-sesamin, (-)-aschantin, (+)-yatein, (+)-dihydroclusin, (+)-burseran, and (-)-isostegane

Synthesis

Volumn , Issue 4, 2002, Pages 515-522

  Enders, Dieter ^a   Lausberg, Vivien ^a   Del Signore, Giuseppe ^a   Berner, Otto Mathias ^a  

^a RWTH AACHEN UNIVERSITY   (Germany)

Author keywords

Aldol reaction; Asymmetric synthesis; Chiral auxiliary; Lignans; amino nitriles

Indexed keywords

PURIFICATION; STEREOCHEMISTRY;

ENANTIOSELECTIVE;

SYNTHESIS (CHEMICAL);

3 (3,4 METHYLENEDIOXYBENZYL) 4 (3,4,5 TRIMETHOXYBENZYL)TETRAHYDROFURAN; ASCHANTINE; DIHYDROCLUSIN; FURAN DERIVATIVE; GAMMA BUTYROLACTONE DERIVATIVE; ISOSTEGANE; LIGNAN DERIVATIVE; LITHIUM CHLORIDE; METHYL GROUP; METHYL PIPERITOL; NITRILE; SESAMIN; TETRAHYDROFURAN; UNCLASSIFIED DRUG; YATEIN;

ARTICLE; ASYMMETRIC SYNTHESIS; CHEMICAL REACTION; DIASTEREOISOMER; ENANTIOSELECTIVITY; PURIFICATION; STEREOCHEMISTRY;

EID: 0036193542     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-20967     Document Type: Article

References (47)