A new approach to the pancratistatin C-ring from d-glucose: Ferrier rearrangement, pseudoinversion and Pd-catalyzed cyclizations
GK Friestad, BP Branchaud
Index: Friestad, Gregory K.; Branchaud, Bruce P. Tetrahedron Letters, 1997 , vol. 38, # 34 p. 5933 - 5936
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Citation Number: 22
Abstract
A Ferrier rearrangement and β-hydroxyketone transposition are key steps in a route to a pancratistatin C-ring precursor. A key feature of the strategy is the pseudoinversion accomplished by β-hydroxyketone transposition, which allows convenient access from methyl α-d-glucopyranoside. Arylations of the C-ring by intramolecular reductive or non- reductive Pd-catalyzed conjugate addition have been demonstrated, utilizing the C1 ...
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