Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans via a two-step sequential Michael-Evans aldol cyclization strategy: total synthesis of (+)-magnolone

Tetrahedron Letters

Volumn 51, Issue 22, 2010, Pages 2975-2978

  Pandey, Ganesh ^a   Luckorse, Srikanth ^a   Budakoti, Asha ^a   Puranik, Vedavati G ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

HWE reaction; Lignans; Magnolone; Michael Evans aldol reaction; Tetrahydrofuran

Indexed keywords

MAGNOLONE; SESAMINONE; SYLVONE; TETRAHYDROFURAN DERIVATIVE; UNCLASSIFIED DRUG;

ANALYTIC METHOD; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; COLUMN CHROMATOGRAPHY; CYCLIZATION; DIHYDROXYLATION; MICHAEL EVANS ALDOL REACTION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

EID: 77951256783     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.03.111     Document Type: Article

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