A new method for the synthesis of α-amino phenylpropanoids under blue light-emitting diode irradiation has been developed through α-C-H benzylation of readily available -phenyl glycine ester with benzyl oxalates as a coupling partner under mild conditions. A range of -phenyl glycine esters were successfully converted to α-amino phenylpropanoid products in moderate to good yields. The utility of this methodology is underlined by its application to the late-state modification of natural products.
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http://dx.doi.org/10.1021/acs.joc.3c01196 | DOI Listing |
Biosci Rep
June 2014
*Department of Plant Biotechnology, College of Agriculture, Shahid Bahonar University of Kerman, P. O. Box: 76169-133, Kerman, Iran.
Safflower (Carthamus tinctorius L.) serves as a reference dicot for investigation of defence mechanisms in Asteraceae due to abundant secondary metabolites and high resistance/tolerance to environmental stresses. In plants, phenylpropanoid and flavonoid pathways are considered as two central defence signalling cascades in stress conditions.
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