## Abstract 3‐Chloroperbenzoic acid‐^17^O,^18^O was prepared from 3‐chlorobenzoyl chloride and hydrogen peroxide‐^17^O,^18^O (obtained by subjecting water‐^17^O,^18^O. Nitrobenzene‐^15^N was reduced to aniline‐^15^N, which was oxidised by 3‐chloroperbenzoic acid to nitrosobenzene‐^15^N. ^15^N and ^
Synthesis of o-, m- and p-Deuterio-, [15N]-and mono[18O]Nitrobenzene
✍ Scribed by Jens H. HøG
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- French
- Weight
- 143 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Synthesis of 0-, mand p-Deuterio-, ["N]and mono[180]Nitrobenzene
📜 SIMILAR VOLUMES
## Abstract The 5‐methyl(^15^N~2~)[__O__^2^,__O__^4^‐^17^O~2~]uridine (= (^15^N~2~)[__O__^2^,__O__^4^‐^17^O ~2~]ribosylthymine; 15) was synthesized and analyzed by ^15^N‐ and ^17^O‐NMR spectroscopy. (^15^N~2~)Urea was condensed with 2,3‐dibromo‐2‐methylpropanoyl chloride (3) and cyclized to form (^
## Abstract __N__‐Methylmorpholine __N__‐(^17^O‐oxide) and __N__‐methylmorpholine __^15^N__‐(^17^O‐oxide) were prepared from __N__‐methylmorpholine and __^15^N__‐methylmorpholine by oxidation with H~2~ ^17^O~2~. The facile one‐pot procedure provided yields of 82 and 76%, respectively. The labeled h
## Abstract For Abstract see ChemInform Abstract in Full Text.