During p r e l i m i n a r y work with u n l a b e l l e d compounds, an attempt was made t o carbonate t h e Grignard r e a g e n t prepared from 2-bromo-2-methylpropane according t o i. No a c i d was i s o l a t e d .
Synthesis of 1,4-dihydro-1-methyl-4-oxonicotinonitrile-8-14C
✍ Scribed by H. E. Johnson; G. R. Waller
- Publisher
- John Wiley and Sons
- Year
- 1968
- Tongue
- French
- Weight
- 177 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
The possibility that I ,4-dihydro-I-methyl-4-oxonicotinonitrile ( V ) is an intermediate in the biosynthesis of the alkaloid ricinine from nicotinic or quinolinic acid in Ricinus communis L. led to our interest in preparing the carbon-14 labeled compound. The 4oxonicotinonitrile ( V ) and the corresponding 6-oxonicotinonitrile were shown to be oxidation products of nicotinonitrile methiodide by a crude enzyme preparation from castor seedlings ( 1 , i ) . The 6-oxonicotinonitrile was shown to be identical to the alkaloid nudiflorine isolated,from Trewia nudiflora (3).
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