𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Beckmann rearrangement of N-(α-hydroxyiminoalkylphosphonyl)amino acids. A convenient synthetic approach to novel peptide-transition-state analogs.

✍ Scribed by Eli Breuer; Hisham Zaher; Zeev Tashma


Publisher
Elsevier Science
Year
1992
Tongue
French
Weight
131 KB
Volume
33
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Use of the Wolff Rearrangement of Diazo
✍ Christel Guibourdenche; Dieter Seebach; François Natt 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 German ⚖ 696 KB

## Abstract Photolysis and Ag‐benzoate‐catalyzed decomposition of the diazo ketones 2 and 4 derived from Z‐Ala‐OH and Z‐Ala‐Ala‐OH in the presence of oligonucleotide derivatives bearing at the 5′‐terminus an NH~2~ instead of the OH group, or an aminohexyl phosphate group lead to Z‐protected 3‐amino