EventsThe 19th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 19th International Electronic Conference on Synthetic Organic Chemistry
Published date
05 Nov, 2015
Citation
Huong Nguyen Thi Thu, Giang Vo-Thanh, Synthesis of Chiral Thiourea-Phosphine Organocatalysts derived from L-Proline, in Proceedings of The 19th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2015, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-19-a058
Share
Email
Facebook
Twitter
LinkedIn

Synthesis of Chiral Thiourea-Phosphine Organocatalysts derived from L-Proline

Huong Nguyen Thi Thu 1
1. University Paris-Sud
Abstract

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.

Keywords
Manuscript
Chiral phase-transfer catalyzed intramolecular aza-Michael reactions for the asymmetric synthesis of isoindolinones
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?