𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Kinetic Resolution of Racemic 2-Hydroxy-γ-butyrolactones by Asymmetric Esterification Using Diphenylacetic Acid with Pivalic Anhydride and a Chiral Acyl-Transfer Catalyst

✍ Scribed by Nakata, Kenya; Gotoh, Kouya; Ono, Keisuke; Futami, Kengo; Shiina, Isamu

Book ID
120019072
Publisher
American Chemical Society
Year
2013
Tongue
English
Weight
590 KB
Volume
15
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Kinetic Resolution of the Racemic 2-Hydr
Kinetic Resolution of the Racemic 2-Hydroxyalkanoates Using the Enantioselective Mixed-Anhydride Method with Pivalic Anhydride and a Chiral Acyl-Transfer Catalyst
✍ Isamu Shiina; Kenya Nakata; Keisuke Ono; Masuhiro Sugimoto; Akihiro Sekiguchi 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 410 KB

## Abstract A variety of optically active 2‐hydroxyalkanoates and the corresponding 2‐acyloxyalkanoates are produced by the kinetic resolution of racemic 2‐hydroxyalkanoates by using achiral 2,2‐diarylacetic acid with hindered carboxylic anhydrides as the coupling reagents. The combined use of diph

An effective kinetic resolution of racem
An effective kinetic resolution of racemic α-arylpropanoic acids, α-arylbutanoic acids, and β-substituted-α-arylpropanoic acids with bis(9-phenanthryl)methanol as a new achiral nucleophile in the asymmetric esterification using carboxylic anhydrides and the acyl-transfer catalyst
✍ Kenya Nakata; Yu-suke Onda; Keisuke Ono; Isamu Shiina 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 562 KB

An effective kinetic resolution of racemic a-arylpropanoic acids, a-arylbutanoic acids, and b-substituted-a-arylpropanoic acids with bis(9-phenanthryl)methanol as a new achiral nucleophile in the asymmetric esterification using carboxylic anhydrides and the acyl-transfer catalyst