En route toward squalestatins and analogues from furfuryl alcohol and maleic anhydride

The Diels-Alder adduct of furfuryl alcohol and maleic anhydride was converted into a 3,4,5-trihydroxy-9-oxo-8-oxabicyclo[4.3.0]non-1 (6)-ene-2-carboxylic derivative, then into polyhydroxylated systems containing three contiguous, oxidized, one-carbon side-chains that are potential intermediates in the synthesis of 6-epi-squalestatins and analogues. (C) 1999 Elsevier Science Ltd. All rights reserved.


Published in:
Tetrahedron Letters, 40, 30, 5499-5502
Year:
1999
ISSN:
0040-4039
Keywords:
Note:
Univ Lausanne, BCH, Chim Sect, CH-1015 Lausanne, Switzerland.
Laboratories:




 Record created 2005-11-09, last modified 2018-03-17


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