## Abstract The reactions of N‐dichlorophosphoryl‐P‐trichlorophosphazene (Cl~3~PNPOCl~2~) with phenylmagnesium chloride, o‐tolylmagnesium chloride, p‐tolylmagnesium chloride, p‐chlorophenylmagnesium chloride, 2‐mesitylmagnesium bromide, and 2‐thienyl lithium were studied. The resulting pentaaryl
The reaction OF N-dichlorophosphoryl- P-trichlorophosphazene with alkyl grignard reagents
✍ Scribed by F. Aslan; A. I. Ozturk; M. Arslan
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 71 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.10153
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✦ Synopsis
Abstract
The reactions of N‐dichlorophosphoryl‐P‐trichlorophosphazene Cl~3~PNP(O)Cl~2~ (1) with benzylmagnesium bromide, 2‐phenylethylmagnesium bromide, trimethylsilylmethylmagnesium chloride, n‐butylmagnesium bromide, cyclohexylmagnesium bromide, cyclopentylmagnesium bromide, tert‐butylmagnesium bromide, iso‐propylmagnesium bromide, and ethylmagnesium bromide were studied. Tri‐ and pentaalkyl phosphazenes were obtained in very poor yield from trimethylsilylmethylmagnesium chloride and cyclohexylmagnesium bromide, respectively. Trialkylphosphoryl compounds formed from benzyl‐, 2‐phenylethyl‐, and n‐butylmagnesium bromide. No phosphorus compound could be isolated from the reaction of 1 with t‐butyl‐, cyclopentyl‐, iso‐propyl‐, and ethylmagnesium bromide. © 2003 Wiley Periodicals, Inc. Heteroatom Chem 14:413–416, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10153
📜 SIMILAR VOLUMES
Nickel-and palladium-catalyzed cross-coupling reactions of organic halides with organometallic reagents is one of the most versatile carbon±carbon bond-forming reactions in organic synthesis. [1] In most cases, aryl and vinyl halides are employed as organic halides, yielding sp 2 ±sp, sp 2 ±sp 2 , a
Nickel-and palladium-catalyzed cross-coupling reactions of organic halides with organometallic reagents is one of the most versatile carbon±carbon bond-forming reactions in organic synthesis. [1] In most cases, aryl and vinyl halides are employed as organic halides, yielding sp 2 ±sp, sp 2 ±sp 2 , a
## Abstract For Abstract see ChemInform Abstract in Full Text.
It has been established by chemical (2a) and CIDNP (3,4) techniques that some transition metal salts catalyze the reaction of Grignard reagents with alkyl halides by a mechanism involving free radicals. Such catalysis is probably responsible for the Wurtz coupling side reaction which lowers the yiel
## Abstract Alkyl sulfoxides were synthesized in good yields from the reaction of alkanesulfinyl chloride with Grignard reagents in the presence of zinc chloride.