Header menu link for other important links
X
Total synthesis of (±)-pentenomycin
Published in
2006
Volume: 47
   
Issue: 30
Pages: 5251 - 5253
Abstract
A concise stereoselective route to (±)-pentenomycin 1 in 33% overall yield starting from the readily accessible Diels-Alder adduct 4 is reported. The key reaction involves decarbonylation of β-methoxy-α,β-unsaturated aldehyde 8 obtained from β-hydroxy-dimethylketal 6. © 2006 Elsevier Ltd. All rights reserved.
About the journal
JournalTetrahedron Letters
ISSN00404039