𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Regioselectivity in the glutathione-phenylglycidyl ether reaction: 1H NMR characterization of the adduct

✍ Scribed by André De Bruyn; Denis De Keukeleire; Elfride van Den Eeckhout; Willy Baeyens

Book ID
101766043
Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
213 KB
Volume
92
Category
Article
ISSN
0037-9646

No coin nor oath required. For personal study only.

✦ Synopsis

A detailed 360 MHz ' H NMR analysis leads to the unambiguous structural identification of the compound , which is regioselectivelv formed in the chemical and enzymatical reactions between glutathione and phenvlqlycidyl ether. The thiol group attacks preferentially the least substituted oxirane carbon atom.

📜 SIMILAR VOLUMES

Characterization of macromolecule resona
Characterization of macromolecule resonances in the 1H NMR spectrum of rat brain
✍ Kevin L. Behar; Takashi Ogino 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 628 KB

## Abstract The ^1^H NMR spectrum of the macromolecule fraction of rat brain cytosol was investigated following centrifugation and dialysis to remove low molecular weight metabolites and peptides (<3500 daltons). At least seven well resolved resonances were detected between 0.9 and 3.0 ppm in the ^