209404-18-2Relevant academic research and scientific papers
Synthesis of isoflavonoids. Enantiopure cis- and trans-6a-hydroxypterocarpans and a racemic trans-pterocarpan
Van Aardt, Theunis G,Van Rensburg, Hendrik,Ferreira, Daneel
, p. 7113 - 7126 (2007/10/03)
Aldol condensation between phenylacetates and benzaldehydes affords 2,3-diaryl-3-hydroxypropanoates which serve as common precursors to both the first racemic trans-pterocarpan and enantiopure cis- and trans-6a-hydroxypterocarpans.
Direct synthesis of pterocarpans via aldol condensation of phenylacetates with benzaldehydes
Van Aardt, Theunis G.,Van Rensburg, Hendrik,Ferreira, Daneel
, p. 11773 - 11786 (2007/10/03)
Aldol condensation between phenylacetates and benzaldehydes affords 2,3- diaryl-3-hydroxypropanoates which are convened into pterocarpans via stepwise deprotection and cyclization in moderate to high yields.
The first direct synthesis of pterocarpans via aldol condensation of phenylacetates with benzaldehydes
Van Aardt, Theunis G.,Van Heerden, Pieter S.,Ferreira, Daneel
, p. 3881 - 3884 (2007/10/03)
Aldol condensation between phenylacetates and benzaldehydes affords 2,3- diaryl-3-hydroxypropanoates which are converted into pt pans in moderate to high yields.
