Title of article :
First synthesis and determination of the absolute stereochemistry of iso-cladospolide-B and cladospolides-B and C
Author/Authors :
Sharma، نويسنده , , G.V.M. and Laxmi Reddy، نويسنده , , K. and Janardhan Reddy، نويسنده , , J.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2006
Abstract :
The syntheses of iso-cladospolide-B, cladospolide-B and cladospolide-C are reported with 4S,5S,11S-configuration. Of the three stereogenic centres, the C-4/C-5 vic-diol was created by Evans aldol condensation, while the C-11 stereocentre was created by Jacobsen’s method. The synthesis of cladospolides 1–3 defined the absolute stereochemistry of these natural products.
Keywords :
Aldol condensation , vic-Diol , Jacobsen’s method , Macrolactonisation , Seco-acid
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters