## Abstract A synthetic procedure for 2‐^14^C‐N‐nitrosohexamethyl‐eneimine 1‐aza‐l‐nitroso‐(2‐^14^C)‐cycloheptane is presented. The starting material was 1‐^14^ C‐cyclohexanone which underwent ring expansion, reduction, and finally nitrosation. The synthesis resulted in a product in good yield (68%
The synthesis of 14C-eugenol and isoeugenol labeled in the methoxy position
✍ Scribed by J. L. Rabinowitz; J. E. Weinberg; A. R. Gennaro; M. Zanger
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- French
- Weight
- 144 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Methylation under pressure of o‐allyloxyphenol with ^14^C‐metheyl iodide was successfully used for the synthesis of ^14^C‐eugenol and isoeugenol labeled in the methoxy position. Eugenol and isoeugenol are important compounds in the practice of dentistry.
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