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Thermal and photochemical reactions of a stable thiobenzaldehyde, 2,4,6-tri-t-butylthiobenzaldehyde

✍ Scribed by Renji Okazaki; Akihiko Ishii; Nobuo Fukuda; Hiroyuki Oyama; Naoki Inamoto


Book ID
104232491
Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
200 KB
Volume
25
Category
Article
ISSN
0040-4039

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✦ Synopsis


Thermal and photochemical reactions of the title compound gave benzothiolane g in high yield; the reaction with free radicals also afforded 2 along with some other products.

We have recently reported the synthesisof the first stable thiobenzaldehyde, 2,4,6-tri-t-butylthiobenzaldehyde (L).' The ready availability and thermal stability of & enable us to study the chemical reactivities of the thioaldehyde about which only little has been known so far.

2 3 Recent papers on some reactions of thioaldehydes prompted us to report our preliminary results


πŸ“œ SIMILAR VOLUMES


Synthesis, Structure, and Reactions of t
✍ Nobuhiro Takeda; Prof. Dr. Norihiro Tokitoh; Prof. Dr. Renji Okazaki πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 996 KB

The first rotational isomers of thiobenzaldehydes, TbtCH=S (2a and 2b: Tbt = 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl), were synthesized and isolated as stable crystalline compounds by the desulfurization of the corresponding overcrowded cyclic polysulfides TbtCHS, (n = 5 or 8) with phosphine rea