Thermolysis, photolysis, and oxidation of an overcrowded 1,3,2-dithiastannetane derivative
✍ Scribed by Norihiro Tokitoh; Verena Stresing; Yasusuke Matsuhashi; Renji Okazaki
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 430 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1042-7163
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✦ Synopsis
Abstract
Reactions of a sterically crowded 1,3,2‐dithiastannetane derivative bearing 2,4,6‐tris[bis(trimethylsilyl)methyl]phenyl (=Tbt) and 2,4,6‐triisopropylphenyl (=Tip) groups on the tin atom are described. Both thermolysis and photolysis of the 1,3,2‐dithiastannetane [Tbt(Tip)SnS~2~CPh~2~] resulted in the formation of products derived from the corresponding stannanethione [Tbt(Tip)Sn=S], while the oxidation reaction by m‐chloroperbenzoic acid gave a novel tincontaining heterocyclic system, an 1,2,4,5‐oxadithiastannolane derivative.
📜 SIMILAR VOLUMES
The thermolysis and photolysis of various oxazoles, diazoles and triazoles 1 have'been reported (la,lb) to generate labile 1,3-dipoles (nitrenes) z which subsequently rearrange to cumulene structures 3 or react with certain dipolar-ophiles (when present) to yield 1,3-dipolar adducts 4. Z=
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Thermal reactions of 3-phenyl-5-arylamino-1,2,4-oxadiazoles I and II were investigated. Neat heating at ca. 250ЊC for 6 hours afforded H 2 O, benzonitrile, arylcyanamides, arylamines, azobenzene, benzimidazole derivatives, and 3,3Ј-diphenyl-5,5Ј-bis[1,2,4-oxadiazolyl]. Analogous results were obtaine