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Enantioselective Rearrangement of Proline Sulfonamides: An Easy Entry to Enantiomerically Pure α-Aryl Quaternary Prolines

✍ Scribed by Francesca Foschi; Prof. Dr. Dario Landini; Dr. Vittoria Lupi; Voichiţa Mihali; Dr. Michele Penso; Dr. Tullio Pilati; Dr. Aaron Tagliabue

Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
244 KB
Volume
16
Category
Article
ISSN
0947-6539

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ChemInform Abstract: Enantioselective Re
ChemInform Abstract: Enantioselective Rearrangement of Proline Sulfonamides: An Easy Entry to Enantiomerically Pure α-Aryl Quaternary Prolines.
✍ Francesca Foschi; Dario Landini; Vittoria Lupi; Voichita Mihali; Michele Penso; 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB

## Abstract A highly enantioselective rearrangement of proline‐derived sulfonamides proceeds in the presence of base to give α‐arylprolines with a quaternary stereocenter in up to 96% optical purity.