## Abstract Results are reported on the regioselective C‐deuteriation of a series of enolates derived from the addition of sec‐BuLi to a variety of substituted amides. The outcomes of the reactions are discussed in terms of the structural nature of the amides and the deuteriated sources employed. C
Synthesis of deuteriated benzaldehydes
✍ Scribed by Keiko Ishimoto; Takehito Tsukinoki; Otohiko Tsuge; Masashi Tashiro
- Book ID
- 102371177
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 257 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A new method for the preparation of d~1~‐benzaldehydes from α‐keto acids in 2 steps is reported.
📜 SIMILAR VOLUMES
## Abstract (13–^2^H) 13‐Demethylretinal, (11,12,13‐^2^H,) 13‐demethylretinal, (9‐^2^H)9‐demethylretinal and (9,10‐^2^H~2~)9‐demethylretinal were prepared in all‐__E__, 9__Z__, 11__Z__ and 13__Z__ isomeric form with high deuterium incorporation. In the synthesis of (9,10‐^2^H~2~)9‐demethylretinal,
An efficient and practical laboratory synthesis of a series of 2-deuterio-2-arylpropionic acids (a-deuterioprofens) is described. The levels of deuterium incorporation are high and the products are synthetically useful.