𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Preparation of 1-O-acylglucuronides of 13C-labelled (R)- and (S)-ketoprofens

✍ Scribed by Kazuki Akira; Tadaaki Taira; Hiroshi Hasegawa; Yoshihiko Shinohara


Publisher
John Wiley and Sons
Year
1997
Tongue
French
Weight
460 KB
Volume
39
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Preparation of [1-14C] and 35S-labelled
✍ Andrew J. Taylor; Anthony H. Olavesen; Colin James 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 French ⚖ 211 KB

Und yl, dodecyl and hexadecyl sulphonates were prepared w i t h y&-label i n t h e 1 -p o s i t i o n . The syntheses r e q u i r e t h e f o r m a t i o n o f a Grignard intermediate from t h e appropriate n-1 a l k y l bromide f o l l o w e d by c a r b o x y l a t i o n o f t h e Grignard w i t h

Bisphosphonic compounds. I. Preparation
✍ Vepsäläinen Jouko; Nupponen Heikki; Pohjala Esko 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 French ⚖ 229 KB

## Abstract Tetrakis(1‐methylethyl) (methylene‐^13^C)bisphosphonate was obtained from ^13^C‐methyliodide via the Michaelis‐Arbuzov reaction with tris(1‐methylethyl)phosphite followed by condensation with chlorophosphonic acid bis(1‐methylethyl)ester. Tetrakis(1‐methylethyl) (methylene‐^14^C)bisphos

Preparation of 2H- and 13C-labelled prec
✍ František Tureček 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 French ⚖ 373 KB

Czechoslovakia 2-=Vinylbicyclo L2.2. lJhept-5--2-0ls, specif i d l y labelled w i t h % at C-3 and in the vinyl group wre p m f m bicyclof2~.2.l]hept-5-en-2-ane in several steps. 13 13 [4-C]oct-l-en-3was prepared in five steps fran These curpow& serve as precursors for the preparatim of c02. specifi

Syntheses of [2-13C] and [1,2-13C] label
✍ Jack E. Baldwin; Robert M. Adlington; Mark A. Russell; Christopher J. Schofield; 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 French ⚖ 353 KB

The syntheses of a-ketoC2-' 3C]glutaric acid and a-ketoC1,2-' 'Cl glutaric acid were each achieved from commercial "CH,I in 5 steps. CH,NO,, prepared in situ from "CH,I and AgNO,, was treated with magnesium methyl carbonate, followed by acidified methanol to give 0,N13CH,C0,CH3. Michael addition to