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Synthesis 1992; 1992(1/2): 123-127
DOI: 10.1055/s-1992-34173
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New Applications of 1,5-Hydrogen Atom Transfer Reactions: Self-Oxidizing Protecting Groups

Dennis P. Curran* , Hosung Yu
  • *Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania, 15260, USA
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Publication History

Publication Date:
18 September 2002 (online)

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Three new alcohol protecting groups are introduced: o-bromobenzyl, o-bromo(methylenedioxy)benzyl, and o-bromotrityl. Removal of these protecting groups under reductive conditions with tributyltin hydride is coupled with an oxidation of the substrate to produce directly an aldehyde or ketone. This oxidation occurs by 1,5-hydrogen transfer, followed by ß-fragmentation. For example, treatment of the o-bromobenzyl ether of 3-phenyl-1-propanol with tibutyltin hydride at 0.001 M (80°C) directly produces 3-phenyl-1-propanal. An application to the selective oxidation of primary alcohols in the presence of secondary alcohols is also introduced.

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