𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Asymmetric halogenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure α-amino acids.

✍ Scribed by David A Evans; Jon A Ellman; Roberta L Dorow


Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
255 KB
Volume
28
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


A general approach to the enantiomeric s
✍ George Kokotos; JoséM. Padrón; Caterina Noula; William A. Gibbons; Victor S. Mar 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 620 KB

A general methodology for the synthesis of saturated lipidic amino acids based on the oxidative cleavage of amino diols obtained by the regioselective opening of enantiomerically enriched 2,3-epoxy alcohols is described. The method opens the way to the synthesis of the enantiomers of lipidic 2-amino

Asymmetric Synthesis Employing a Chiral
✍ Oliver Achatz; Andrea Grandl; Klaus Theodor Wanner 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 423 KB 👁 1 views

A new asymmetric synthesis of disubstituted α-amino acids From the major diastereomers 17c-d the corresponding αamino acids 19c-d are obtained enantiomerically pure upon is presented. This synthesis is based on the chiral 5-methoxy-1,4-oxazin-2-one derivative 5 relying on the α-hydroxy acid hydroly