Title of article
Studies towards diarylheptanoid synthesis. Part 1: Synthesis and ring cleavage reactions of hexahydro-2H,5H-pyrano[2,3-b]pyran-2-ones
Author/Authors
Li، نويسنده , , Wei and Mead، نويسنده , , Keith T. and Smith، نويسنده , , Laura T.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2003
Pages
3
From page
6351
To page
6353
Abstract
Lewis acid promoted anomeric substitution reactions of a stereoselectively prepared hexahydro-2H,5H-pyrano[2,3-b]pyran-2-one derivative was studied as a model for diarylheptanoid synthesis. Aromatic nucleophiles consistently provided the expected thermodynamic C-aryl pyranoside product.
Keywords
blepharocalyxin , oxocarbenium ion , hexahydro-2H , 3-b]pyran-2-one , C-aryl pyranoside , diarylheptanoid
Journal title
Tetrahedron Letters
Serial Year
2003
Journal title
Tetrahedron Letters
Record number
1653999
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