𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective Reduction of Enantiopure β-Enamino Esters by Hydride: A Convenient Synthesis of Both Enantiopure β-Amino Esters

✍ Scribed by Cimarelli, Cristina; Palmieri, Gianni


Book ID
120085075
Publisher
American Chemical Society
Year
1996
Tongue
English
Weight
312 KB
Volume
61
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Chiral cyclic β-amino esters. Part II: S
✍ J. Blot; A. Bardou; C. Bellec; M.-C. Fargeau-Bellassoued; J.P. Célérier; G. Lhom 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 182 KB

Catalytic and chemical reductions of chiral pyrrolidine 13-enamino esters provides corresponding [3-amino esters with good to moderate diastereomer excesses. The unexpected major diastereomer 5 comes from a reduction process which amounts to an anti hydrogen addition.