𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reactivity of N-benzoyl-N-phenylhydroxylamine in cationic micellar media for the cleavage of carboxylate and phosphate esters

✍ Scribed by Kumar, Birendra; Tikariha, Deepti; Ghosh, Kallol K.


Book ID
122114751
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
677 KB
Volume
193
Category
Article
ISSN
0167-7322

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Hydrolysis of carboxylate and phosphate
✍ Namrata Singh; Kallol K. Ghosh; Jan Marek; Kamil Kuca 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 266 KB

## Abstract The reactions of __p__‐nitrophenyl acetate (PNPA) with a series of monopyridinium oximes, viz. 2‐PAM (2‐hydroxyiminomethyl‐1‐methylpyridinium iodide), 3‐PAM (3‐hydroxyiminomethyl‐1‐methylpyridinium iodide), and 4‐PAM (4‐hydroxyiminomethyl‐1‐methylpyridinium iodide) have been studied in

Kinetics and mechanism for the formation
✍ M. Niyaz Khan 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 141 KB 👁 1 views

The rate of cleavage of ethyl N-[o -(N-methyl-N-hydroxycarbamoyl)benzoyl]carbamate (ENMBC) in the buffer solutions containing N-methylhydroxylamine, acetate + Nmethylhydroxylamine, and phosphate + N-methylhydroxylamine followed an irreversible consecutive reaction path: ENMBC k 1 obs → A k 2 obs → B