A novel class of thiourea-phosphine was prepared from L-Proline as a chiral renewable resource. The original structure of the chiral framework offers an interesting potential to the construction of bifunctional organocatalysts for asymmetric transformations.
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The dependence of the 1,2-disubstituted propanes X-C1H12-C2H2(Y)-C3H33 methyl protons (C3H33) chemical shifts on the nature of substituents X in the 1H NMR spectra. An anomeric effect action?Next Article in session
Synthesis of Chiral Thiourea-Phosphine Organocatalysts derived from L-Proline
Published: 05 November 2015 by MDPI in The 19th International Electronic Conference on Synthetic Organic Chemistry session General Organic Synthesis