๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Synthesis of Orthogonally Protected ( R )- and ( S )-2-Methylcysteine via an Enzymatic Desymmeterization and Curtius Rearrangement

โœ Scribed by Kedrowski, Brant L.


Book ID
126285650
Publisher
American Chemical Society
Year
2003
Tongue
English
Weight
61 KB
Volume
68
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Enantioselective synthesis of benzylic s
โœ Elisabetta Brenna; Claudio Fuganti; Francesco G. Gatti; Massimo Passoni; Stefano ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 145 KB

The Johnson-Claisen rearrangement of enantiopure allylic alcohols in triethylorthopropionate is the key step for the preparation of chiral molecules with benzylic stereogenic carbon atoms bearing an isopropyl moiety. The synthetic procedure is applied to the preparation of (R)-and (S)-3-methyl-2-phe