Photolabile protection of 1,2- and 1,3-diols with salicylaldehyde derivatives

Org Lett. 2008 Nov 20;10(22):5277-80. doi: 10.1021/ol802141g. Epub 2008 Oct 22.

Abstract

1,2- and 1,3-diols, including carbohydrates, can be readily caged as acetals of 5-methoxy- or 5-hydroxysalicylaldehydes. Irradiation of these acetals with 300 nm light results in their efficient (Phi = 0.2-0.3) cleavage, regenerating an aldehyde and a glycol in excellent chemical yield. Photoreactive 5-hydroxysalicylaldehyde acetals can be produced by mild in situ reduction of photostable p-quinone precursors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetals / chemistry
  • Alcohols / chemistry*
  • Aldehydes / chemistry*
  • Photochemistry

Substances

  • Acetals
  • Alcohols
  • Aldehydes
  • salicylaldehyde