Stereoselective preparation of trisubstituted (Z)-alkenes; synthesis of the C17-C27 fragment of (-)-laulimalide

Tetrahedron

Volumn 61, Issue 8, 2005, Pages 1971-1979

  Uenishi, Jun'ichi ^a   Ohmi, Masashi ^a   Matsui, Katsuaki ^a   Iwano, Megumi ^a  

^a KYOTO PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

( ) Laulimalide; 3,6 Dihydro 2H pyran; Bromoenyne; SN2 reaction; Trisubstituted (Z) alkene

Indexed keywords

3,6 DIHYDRO[2H]PYRAN; ALKENE DERIVATIVE; ALKYNE DERIVATIVE; ALLYL COMPOUND; CARBON; KETONE DERIVATIVE; LAULIMALIDE; MESYLIC ACID DERIVATIVE; PHOSPHONIC ACID DERIVATIVE; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLIZATION; DRUG SYNTHESIS; GRIGNARD REACTION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HORNER WADSWORTH EMMONS REACTION; MOLECULAR INTERACTION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STEREOSPECIFICITY;

EID: 13444257629     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.01.002     Document Type: Article

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