𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Investigation of new chiral 1,3-oxazolidine-2-thiones: analytical separation and optical resolution of racemic carboxylic acids and amino acids

✍ Scribed by Nagao, Yoshimitsu; Kumagai, Toshio; Yamada, Shozo; Fujita, Eiichi; Inoue, Yoshinori; Nagase, Yunosuke; Aoyagi, Sakae; Abe, Takao

Book ID
121204690
Publisher
Royal Society of Chemistry
Year
1985
Weight
944 KB
Category
Article
ISSN
1472-7781

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and optical resolution of 1-[(
Synthesis and optical resolution of 1-[(3-carboxy-1,1′-biphenyl)-2-yl]-1H-pyrrole-2-carboxylic acid
✍ Ferenc Faigl; Bernadett Vas-Feldhoffer; Veronika Kudar; Mátyás Czugler; Krisztin 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 295 KB

## Abstract Site selective mono‐ and dimetalation methods have been developed for the functionalization of 1‐[(1,1′‐biphenyl)‐2‐yl]‐1H‐pyrrole. Optical resolution of the prepared 1‐[(3‐carboxy‐1,1′‐biphenyl)‐2‐yl]pyrrole‐2‐carboxylic acid provided new atropisomeric 1‐arylpyrrole derivatives. The ab

Lewis acid activation of chiral 2-triflu
Lewis acid activation of chiral 2-trifluoromethyl-1,3-oxazolidines. Application to the stereoselective synthesis of trifluoromethylated amines, α- and β-amino acids
✍ Nicolas Lebouvier; Christophe Laroche; Florent Huguenot; Thierry Brigaud 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 84 KB

The reaction of chiral 2-trifluoromethyl-1,3-oxazolidines with various silylated nucleophiles under Lewis acid activation provides a stereoselective route to functionalized a-trifluoromethylamines. This methodology was successfully applied to the diastereoselective synthesis of trifluoromethylated h