𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Total synthesis of [7-14C]-(±)-colchicine

✍ Scribed by Renée Pontikis; Nguyen Hoang Nam; Henri Hoellinger


Publisher
John Wiley and Sons
Year
1989
Tongue
French
Weight
479 KB
Volume
27
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


The synthesis of (*)-colchicine 1. labelled with carbon-14 at the 7position of the B ring was achieved by a sixteen step sequence with an overall radiochemical yield of 2.5% from [Ba14C03] (Specific activity : 55 m(li-mmol-1).


📜 SIMILAR VOLUMES


Synthesis of geraniol-7−14C
✍ H. D. Durst; E. Leete 📂 Article 📅 1971 🏛 John Wiley and Sons 🌐 French ⚖ 201 KB

Gerani01-7-~~C has been synthesized in an overall yield of 46 x, starting with acetone-2-14C. INTRODUCTION.

Synthesis of 14C-labeled 7α-methoxycepha
✍ Kazuharu Tamazawa; Hideki Arima 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 French ⚖ 295 KB 👁 1 views

## Abstract [Caboxamido‐^14^C]Cefotetan, 7α‐[4‐(carbamoyl carboxymethylene)‐1,3‐dithietan‐2‐yl] [^14^C]carboxamido‐7α‐methoxy‐3‐(1‐methyl‐1H‐tetrazol‐5‐yl)thiomethyl‐y1)thiomethyl‐3‐cephem‐4‐carboxylic acid (IX), a new cephamycin derivative, was synthesized from bromo[1‐^14^C]acetic acid for metabo

Synthesis of DL-[7-14C]indospicine and D
✍ Elzbieta Wieczorkowska; Mervyn P. Hegarty 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 French ⚖ 322 KB

A new method of synthesis of DL-[ 7-14C]indospicine and DL-2-amino-[ 7-1 4C]pimelic acid and their nonradioactive equivalents is reported. The combined radiochemical yield of both compounds, starting from potassium 1 14C]cyanide was 15.3%. Indospicine was isolated as the flavianate.

Synthesis of daunorubicin-14-14C and adr
✍ C. Rolland Chen; Mary Tan Fon; Alan N. Fujiwara; David W. Henry; Morris A. Leaff 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 French ⚖ 275 KB

## Abstract Reaction of adriamycinone with excess ^14^CH~3~Mgl and periodate cleavage of the resulting glycol (5) affords daunomycinone‐14‐^14^C (6). Bromination and hydrolysis of 6 gives adriamycinone‐14‐^14^C (8). Coupling of 6 and the 14‐0‐p‐anisyldiphenyl‐methyl derivative (9) with 1‐chloro‐3‐N