Cyclic SN compounds and phosphorus reagents: Part X. Synthesis and characterization of phosphinimino-substituted SN heterocycles
β Scribed by C. J. Thomas; M. N. Sudheendra Rao
- Book ID
- 102846526
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 558 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1042-7163
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β¦ Synopsis
R o o m temperature reactions o f S f l , with (amino) diphenylphosphines, (R)Ph2P, have basically yielded two different types of S-N heterocycles under two different stoichiometric conditions. Phosphiniminocyclotrithiatriazenes, (R)Ph2PN-S3N3 (R = C4H8N-, C5HioN-, C,Hi2N--, CH,NC,H&--, ( C ~H I 1 ) 2 N-, and (C,H jCH2)2N-) have been obtained (yield 45-76%) from a 1 :2 mole ratio (S4N4: (R)Ph,P) reaction, while the disubstituted S f l , derivatives, and C,H12N-) have been obtained (yield 30-45%) only from a I :3.5-4 mole ratio reaction. All the 1,5-[Ph2(R)PNl2S,N4 derivatives prepared in this study undergo a room temperature solution phase transformation to the corresponding (R)Ph2PN-S3N, heterocycles.
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## Abstract The reaction of indole with cyclohexanone in the presence of the Lewis acid, boron trifluoride diethyl etherate, resulted in the synthesis of a novel and interesting product (**1**) in addition to the bis(indolyl)methane system (**2**). The structure of this novel compound has been dete