A facile synthesis of [1-13C]benzonitrile by bromination-dehydrobromination of [1-13C]1-cyanocyclohexene
✍ Scribed by Sun-Shine Yuan; Alfred M. Ajami
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- French
- Weight
- 196 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0022-2135
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📜 SIMILAR VOLUMES
13 C 1 -pinonaldehyde is prepared in seven steps from cis-pinonic acid. In the key sequence, the introduction of labeled carbon is accomplished by Lieben degradation of a methyl ketone followed by treatment of the resultant carboxylic acid with 13 C-methyl lithium.
## Abstract For mass spectrometric studies 1‐phenyl‐2‐phenyl‐1‐^13^C‐ethene‐1‐^13^C (trans‐stilbene) was synthesized from acetic‐1‐^13^C acid and acetic‐2‐^13^C acid via methylcyclohexene‐1‐^13^C and ‐α‐^13^C and toluene‐1‐^13^C and ‐α‐^13^C. No scrambling of the label was observed during the aroma
## Abstract An improved synthesis of [1,1′‐^13^C~2~]‐L‐cystine which includes the optical resolution of the labeled N‐acetyl‐S‐benzyl‐DL‐cysteine by __Aspergillus__ acylase into __S__‐benzyl‐L‐cysteine is described.
13 13 [2-C]cyclohexanone was synthesized through [ Clcyanation of cyclopentanone followed by acetylation, reduction and ring expansion. Treatment with cupric bromide/lithium bromide and dehydrobromination of the resulting labeled 1,6-dibromohexanone in a "one pot" procedure gave [2-13C]phenol.