The introduction of two hydroxy groups with differential protection at the endo positions of C(5) and C(6) of the ''naked sugars of the first generation'' has been achieved by seleno-Pummerer rearrangement of 5-endo-hydroxy-6-exa-phenylseleno-7-oxabicyclo[2.2.1]heptan-2-one derivatives followed by deselenation with Bu(3)SnH.
Type
research article
Authors
Publication date
1995
Published in
Issue
5
Start page
420
End page
422
Note
Univ lausanne,bch dorigny,chim sect,ch-1015 lausanne,switzerland.
Peer reviewed
REVIEWED
EPFL units
Available on Infoscience
November 9, 2005
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