✦ LIBER ✦

Adsorbed alkyl radicals in the cathodic synthesis of mercury dialkyls

✍ Scribed by O.R. Brown; K. Taylor

Book ID: 104149816
Publisher: Elsevier Science
Year: 1974
Weight: 429 KB
Volume: 50
Category: Article
ISSN: 0022-0728
DOI: 10.1016/s0022-0728(74)80152-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The Nature of Mercury-Carbon Bonds in Me

The Nature of Mercury-Carbon Bonds in Mercury Alkyl Radicals

✍ Gowenlock, B. G.; Polanyi, J. C.; Warhurst, E. 📂 Article 📅 1953 🏛 The Royal Society 🌐 English ⚖ 575 KB

The role of quinidine in induction of as

The role of quinidine in induction of asymmetric synthesis at mercury cathodes

✍ E. Kariv; H.A. Terni; E. Gileadi 📂 Article 📅 1973 🏛 Elsevier Science 🌐 English ⚖ 894 KB

ChemInform Abstract: Radical Alkylation

ChemInform Abstract: Radical Alkylation in the Synthesis of Phenacylfurans.

✍ V. T. Abaev; K. V. Bosikova; O. V. Serdyuk; A. V. Butin 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 22 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Stereochemistry of electroreductions of

Stereochemistry of electroreductions of bromocyclopropanes: 1-asymmetric electrochemical synthesis by reduction at a mercury cathode in the presence of adsorbed alkaloïds

✍ R. Hazard; S. Jaouannet; A. Tallec 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 685 KB

Dialkyl and Methyl-Alkyl Zirconocenes: S

Dialkyl and Methyl-Alkyl Zirconocenes: Synthesis and Characterization of Zirconocene-Alkyls That Model the Polymeryl Chain in Alkene Polymerizations

✍ Klamo, Sara B.; Wendt, Ola F.; Henling, Larry M.; Day, Michael W.; Bercaw, John 📂 Article 📅 2007 🏛 American Chemical Society 🌐 English ⚖ 299 KB

Reaction between alkyl isocyanides and d

Reaction between alkyl isocyanides and dialkyl acetylenedicarboxylates in the presence of N-alkyl isatins: convenient synthesis of γ-spiro-iminolactones

✍ Abbas Ali Esmaeili; Masoomeh Darbanian 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 109 KB

The highly reactive 1:1 intermediate generated in the reaction between an alkyl isocyanide and a dialkyl acetylenedicarboxylate is trapped by N-alkyl isatin to yield iminolactones in fairly high yields.