Journal article
C-alkylation reactions of phenylsulphonylnitromethane. A convenient new α-nitro-sulphone synthesis
Journal of the Chemical Society, Chemical Communications, (6)
1980
Abstract
Phenylsulphonylnitromethane (
1
) is
C
-alkylated by benzylic halides and primary alkyl iodides affording
α
-nitro-sulphones in 43-75% yield;
α
-nitro-sulphones (83-90% yield) are also obtained from the corresponding
C
-alkylation of allylic acetates in the presence of catalytic Pd(PPh
3
)
4
.
Metrics
9 Record Views
10 citations in Scopus
Details
- Title
- C-alkylation reactions of phenylsulphonylnitromethane. A convenient new α-nitro-sulphone synthesis
- Creators
- Peter A WadeScott D MorrowSteven A HardingerMallory S SaftHarry R Hinney
- Publication Details
- Journal of the Chemical Society, Chemical Communications, (6)
- Publisher
- Royal Society of Chemistry
- Number of pages
- 2
- Resource Type
- Journal article
- Academic Unit
- [Retired Faculty]
- Scopus ID
- 2-s2.0-33749279275
- Other Identifier
- 991019173776304721