Oxidation of the titled inner salt 1 with a typical one-electron oxidizing reagent, NOPF 6 , produced the radical cation 5a, whose dimerization, followed by loss of a sulfur atom, led to the formation of the bis-carbenium salt 4a in 95% yield. Moreover, reduction of 1 with a typical one-electron red
An Improved Synthesis of Inner Salts, 2,2-Bis(dialkylamino)-2-ethylium-1-dithioates
β Scribed by Keiichi Akimoto; Juzo Nakayama
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 157 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1042-7163
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β¦ Synopsis
The reaction of 1,1-bis(dialkylamino)ethenes ( ) with an equimolar amount of disulfur dichloride in the presence of triethylamine affords the stable inner salts 2,2-bis(dialkylamino)-2-ethylium-1-dithioates (1) in good yields.
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Arsenic analogs of lecithins (i.e. with replacement of nitrogen by arsenic in the choline group) are probably trace constituents of phospholipids in many organisms. Attempts to synthesize 1,2bis(palmitoy1oxy)-3propyl 2-trimethylarsonioethyl phosphate (arsenolecithin) according to wellestablished pro
A fresh look has been taken at the reaction of PCl 3 with thioanisole 1b and AlCl 3 that gives, after treatment with water, the title compounds cis-2b in 38% yield together with small amounts of the isomeric cis-3b (2%). The course of this reaction has been studied by 31 P-NMR spectroscopy. A multis