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Reduction of sulfoxides by dichlorocarbene under phase transfer catalysis conditions

✍ Scribed by H.S.Dilanjan Soysa; William P. Weber


Publisher
Elsevier Science
Year
1978
Tongue
French
Weight
141 KB
Volume
19
Category
Article
ISSN
0040-4039

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✦ Synopsis


The facile and economical generation of dichlorocarbene from the reaction of chloroform with 50% aqueous sodium or potassium hydroxide under phase transfer catalytic conditions has stimulated study of the reactions of dichlorocarbene with numerous types of non-olefinic substrates.' Only one example of the reaction of dichlorocarbene with a sulfoxide has previously been reported. Thus dichlorocarbene generated by reaction of ethyl trichloroacetate with sodium methoxide reacts with dimethylsulfoxide to yield dimethyl sulfide (20%).2


πŸ“œ SIMILAR VOLUMES


Autooxidation of methylheterocycles unde
✍ I. G. Iovel'; Yu. Sh. Gol'dberg; A. P. Gaukhman; R. M. Zolotoyabko; M. V. Shiman πŸ“‚ Article πŸ“… 1991 πŸ› Springer US 🌐 English βš– 312 KB

The autooxidation of methyl-and dimethyl-substituted N-, S-, and O-heterocyclic compound derivatives has been studied in 1,2-dimethoxyethane--t-BuOK in the presence of l8-crown-6. Monoand dicarboxylic acid derivatives of pyrazine, pyridine, pyrimidine, and thiophene have been synthesized. Autooxida