Synthesis of dimethyl 4-thiazolidinylphosphine oxides via addition of dimethylphosphine oxide to 3-thiazolines
✍ Scribed by Harald Gröger; Davoud Tehranfar; Jürgen Martens; Jens R. Goerlich; Holger Thönnessen; Peter G. Jones; Reinhard Schmutzler
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 248 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1042-7163
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✦ Synopsis
The addition of dimethylphosphine oxide and its trimethylsiloxyphosphorus(III) derivative, generated in situ, to 3-thiazolines was found to yield dimethyl 4thiazolidinylphosphine oxides via three different synthetic routes. The structures of two products were confirmed by X-ray analysis; common features include approximate envelope conformations of the five-membered rings and hydrogen bonding of the form N-H• • •OסP.
📜 SIMILAR VOLUMES
Synthesis and Oxidation of Chiral 2-Thiazolines (4,5-Dihydro-1,3thiazoles). -Eight new chiral thiazolines (IV) and (X) are prepared by treatment of oxazolines (III) or alcohols (IX) with P2S5. These thiazolines are oxidized using various agents. -(AITKEN, R. A.; ARMSTRONG, D. P.;