170240-23-0Relevant academic research and scientific papers
Synthesis of β-dimorphecolic acid exploiting highly stereoselective reduction of a side-chain carbonyl group in a π-allyltricarbonyliron lactone complex
Ley, Steven V.,Meek, Graham
, p. 1125 - 1133 (2007/10/03)
A highly enantioselective synthesis of β-dimorphecolic acid 1 is reported. The synthesis features a diastereoselective reduction of the ketone 4, in which the tricarbonyliron lactone tether induces a 1,5 transfer of chirality, followed by a stereoselectiv
Synthesis of β-dimorphecolic acid exploiting highly stereoselective-reduction of a side-chain carbonyl group in a π-allyltricarbonyliron lactone complex
Ley,Meek
, p. 1751 - 1752 (2007/10/02)
A highly stereoselective synthesis of β-dimorphecolic acid is accomplished utilising a π-allyltricarbonyliron lactone complex 3 to control the formation of all the stereochemical features of the natural product.
