𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A selective cathodic reduction of β-chlorovinylimines in N,N′ dimethylformamide

✍ Scribed by R. Saiganesh; K.K. Balasubramanian; C.S. Venkatachalam


Publisher
Elsevier Science
Year
1989
Tongue
French
Weight
188 KB
Volume
30
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


The controlled-potential electrolyses of various subsituted chlorovinylimines, viz., 4-chloro-3-(N-aryliminomethyl)-ZH(l)-benzopyrans in dimethylformamide(DMF) solutions at mercury


📜 SIMILAR VOLUMES


Effect of benzoic acid on the cathodic r
✍ Barbara Kwiatek; Marek K. Kalinowski 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 408 KB

The effect of benzoic acid on the polarographic reduction of two series of aromatic nitro compounds in NJ-dimethylformamide has been investigated. The first reaction series was p-X-C,H,-NO, compounds, whereas the second one comprised mononitroarenes. In the presence of the acid a new cathodic wave

The reduction of alkyl halides at a lead
✍ M. Fleischmann; D. Pletcher; C.J. Vance 📂 Article 📅 1971 🏛 Elsevier Science ⚖ 498 KB

A wide range of metal alkyls has now been prepared electrochemically 1-3. In general, the synthetic procedures involve the electrochemical generation of radicals, either by the reduction of alkyl halides or the oxidation of carbanionic species, at a sacrificial metal electrode. Much of the effort in

The effects of substitution on the elect
✍ Chai-Yu Li; Frederic W. Whitehurst 📂 Article 📅 1982 🏛 Elsevier Science 🌐 English ⚖ 411 KB

The polarographic reduction of 5, 6, 11, 12-naphthacenetetrone (NT) and several of its chloro, methyl, and nitro derivatives were investigated . The electrochemical behavior of NT was compared with 6,11-dihydroxy-5,12-naphthacenequinone (DHNQ) previously studied . Like DHNQ, NT exhibits two reductio

The effects of substitution on the eletr
✍ Chia-Yu Li; Myron L. Caspar; Donald W. Dixon Jr. 📂 Article 📅 1980 🏛 Elsevier Science 🌐 English ⚖ 765 KB

Abstrmct -The electrochemical reduction of 6,11-dihydroxy-5,12-naphthacenequinone (DHNQ) in N,Ndimethylformamide was investigated. Under polarographic conditions, DHNQ behaves like a simple aromatic quinone with reduction occurring in two successive one-electron steps followed by protonation in the