𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of carbon-14 labeled [1-14C]-, and [2-14C]-L-tyrosine

✍ Scribed by W. Augustyniak; R. Kański; M. Kańska


Publisher
John Wiley and Sons
Year
2001
Tongue
French
Weight
96 KB
Volume
44
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


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 [2‐^14^C]cinnamic acid, prepared from potassium [^14^C]cyanate or [2‐^14^C]malonic acid, and by addition of ammonia in the presence of enzyme PAL. The labeled isotopomers of L‐Phe have been converted into [1‐^14^C]‐, and [2‐^14^C]‐L‐Tyr using the enzyme L‐phenylalanine hydroxylase. Copyright © 2001 John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


Synthesis of carbon-14 labeled 1,4-benzo
✍ Richard S. P. Hsi 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 French ⚖ 287 KB 👁 1 views

## Abstract Diazepam‐^14^C and demethyldiazepam‐^14^C are synthesized from glycine‐1‐^14^C. Addition of diketene to diazepam‐^14^C leads to ketazolam‐^14^C. The reaction conditions for the formation of ketazolam from diazepam is studied using high‐pressure liquid chromatography in conjunction with

Synthesis of 14C-labelled isotope-isomer
✍ Ioana Bally; Eugenia Gǎrd; Elieabeta Ciornei; Maria Biltz; A. T. Balaban 📂 Article 📅 1975 🏛 John Wiley and Sons 🌐 French ⚖ 301 KB

## Abstract The synthesis of n‐heptane‐1‐^14^C is described. starting from ^14^CH~3~I via (^14^CH~3~) ~2~Cd and caproyl chloride; for obtaining n‐heptane‐2‐^14^C, n‐pentyl bromide is converted into the Grignard reagent, carbonated with ^14^CO~2~, and the resulted coproic acid is converted into its

Synthesis of carbon-14 labelled l,5 diar
✍ 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

Synthesis and characterization of carbon
✍ C. E. Blackburn; A. J. Glazko 📂 Article 📅 1972 🏛 John Wiley and Sons 🌐 French ⚖ 206 KB

## SYNTtIESIS AHD CHARACTERIZATION OF CARBON-14 LABELLED 4,4'-DIAMINODIPHENYL SULFONE (DAPSONE-l4C; D 3 S -1 4 C > , C.E. B l a c k b u r n and A.J. G l a z k o . D e p a r t m e n t o f P h a r m a c o l o g y . D i v i s i o n of S c i e n t i f i c and M e d i c a l Affairs. P a r k e -D a v i

Synthesis of carbon-14 labelled acetamin
✍ S. Stavchansky; P. Wu 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 French ⚖ 120 KB

## Abstract A simple and convenient method for the condensation of paminophenol (I) with ^14^C‐acetic anhydride (II) yields up to 76% of ^14^C‐labelled 4‐hydroxyphenylacetamide (carbonyl‐^14^C) (III). Typical synthesis time is 60 minutes. Radioactive yield is 51%, and specific activity is 0.22 μCi/

Synthesis of 14C- and 14C3-labelled Org
✍ P. H. G. Wiegerinck; L. W. H. Hofstede; F. M. G. M. Sperling; J. F. Vader 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 French ⚖ 237 KB

## Abstract Org 37462 (1) is the active ingredient in Orgalutran^®^, an innovative product that reduces the time of treatment in __in vitro__ fertilization from four to less than two weeks. Org 37462 is a synthetic decapeptide containing several amino acids that are unnatural in stereochemistry and