𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Syntheses of 2-(diacetoxymethyl-14C)-5-nitrofuran and carbon-14 labeled nitrofurazone

✍ Scribed by Richard I Duclos Jr.; Betty-Ann Hoener

Publisher
John Wiley and Sons
Year
1986
Tongue
French
Weight
253 KB
Volume
23
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of carbon-14 labeled [1-14C]-,
Synthesis of carbon-14 labeled [1-14C]-, and [2-14C]-L-tyrosine
✍ W. Augustyniak; R. Kański; M. Kańska 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 French ⚖ 96 KB 👁 1 views

## Abstract Two labeled isotopomers of L‐tyrosine, L‐Tyr, have been synthesized using specific properties of the enzymes phenylanine ammonia lyase, PAL, and L‐phenylalanine hydroxylase. In an intermediate step [1‐^14^C]‐, and [2‐^14^C]‐L‐phenylalanine, L‐Phe, have been obtained from [1‐^14^C]‐, and

Syntheses of 14C-mustard-labelled and 14
Syntheses of 14C-mustard-labelled and 14C-leucine-labelled Asaley
✍ D. Farquhar; K. Lu; T. L. Loo 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 French ⚖ 429 KB

## Abstract The synthesis of Asaley labelled with ^14^C in the mustard (Asaley‐must‐^14^C) or the leucine (Asaley‐leu‐^14^C) moiety is described. In the former, ethyl pamino‐N^α^‐acetyl‐DL‐phenylalanyl‐L‐leucinate was reacted with ethylene oxide(U)‐^14^C to give the bis(hydroxyethyl)amino analogue,

Synthesis of 5-nitrofuran-2 [14C] aldehy
Synthesis of 5-nitrofuran-2 [14C] aldehyde diacetate and the antibacterial agent [14C]-nifuroxazide
✍ L. F. Elsom; D. R. Hawkins 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 French ⚖ 235 KB

## 14 F u r a n -2 -l CJcarboxylic a c i d h a s been prepared in 74% yield by carbonation of 2-furyllithium. Furan-2-fi4CTaldehyde w a s isolated a s the d i a c e t a t e after c a t a l y t i c reduction of the corresponding a c i d chloride. Nitration g a v e 5nitrofuran-2-[14CJaldehyde dia ce

Synthesis of carbon-14 labelled l,5 diar
Synthesis of carbon-14 labelled l,5 diaryl-[5-14C]-l,2,3-triazolines
✍ Hojatollah Matloubi; Abbas Shafiee; Nader Saemian; Gholamhossein Shirvani; Farib 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 French ⚖ 81 KB

## Abstract Two 1,2,3‐triazoline anticonvulsants, 1‐(4‐methylsulphone‐phenyl)‐5‐(4‐methoxy‐phenyl)‐1,2,3‐triazoline and l‐(4‐methylsulphone‐phenyl)‐5‐phenyl‐1,2,3‐triazoline, both labelled with carbon‐14 in the 5‐position, have been synthesized as part of a 5‐step sequence. Copyright © 2003 John Wi