Reaction of Alkanesulfinyl Chloride with Grignard Reagents: a Convenient Synthesis of Alkyl Sulfoxides
β Scribed by Xiao-Bo Li; Jin-Tao Liu
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 44 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0256-7660
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β¦ Synopsis
Abstract
Alkyl sulfoxides were synthesized in good yields from the reaction of alkanesulfinyl chloride with Grignard reagents in the presence of zinc chloride.
π SIMILAR VOLUMES
Nickel-and palladium-catalyzed cross-coupling reactions of organic halides with organometallic reagents is one of the most versatile carbonΒ±carbon bond-forming reactions in organic synthesis. [1] In most cases, aryl and vinyl halides are employed as organic halides, yielding sp 2 Β±sp, sp 2 Β±sp 2 , a
Nickel-and palladium-catalyzed cross-coupling reactions of organic halides with organometallic reagents is one of the most versatile carbonΒ±carbon bond-forming reactions in organic synthesis. [1] In most cases, aryl and vinyl halides are employed as organic halides, yielding sp 2 Β±sp, sp 2 Β±sp 2 , a
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