✦ LIBER ✦

Reduction of triethyllead cation - a novel route to generate ethyl radicals

✍ Scribed by Chi-Hua Wang; Philip L. Levins; Harry G. Pars

Publisher: Elsevier Science
Year: 1964
Tongue: French
Weight: 175 KB
Volume: 5
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(64)83026-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Fragmentation of oxyalkyl radicals: A ne

Fragmentation of oxyalkyl radicals: A new general route to nitrogen radicals

✍ A.R. Forrester; M. Gill; E.M. Johansson; C.J. Meyer; R.H. Thomson 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 185 KB

ChemInform Abstract: Cu(II)-Mediated Gen

ChemInform Abstract: Cu(II)-Mediated Generation of Triarylamine Radical Cations and Their Dimerization. An Easy Route to Tetraarylbenzidines.

✍ Kesavapillai Sreenath; Chettiyam Veettil Suneesh; Venugopal K. Ratheesh Kumar; K 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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

Novel reduction (Zn-AcOH) of DDHQ esters

Novel reduction (Zn-AcOH) of DDHQ esters. A new route to tropone synthesis

✍ Tirumalai R. Kasturi; Pragnacharyulu V.P. Palle; Jitendra A. Sattigeri; Kaipench 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 334 KB

Intramolecular electrolytic reductive co

Intramolecular electrolytic reductive coupling of activated olefins: a novel route to cyclic compounds

✍ James D. Anderson; Manuel M. Baizer 📂 Article 📅 1966 🏛 Elsevier Science 🌐 French ⚖ 175 KB

A novel route to (±)-aspidospermidine: F

A novel route to (±)-aspidospermidine: First application of “radical-polar crossover” reactions to total synthesis

✍ Owen Callaghan; Christopher Lampard; Alan R. Kennedy; John A. Murphy 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 209 KB

The generation and cyclisation of pyridi

The generation and cyclisation of pyridinium radicals as a potential route to indolizidine alkaloids

✍ Adrian P. Dobbs; Keith Jones; Ken T. Veal 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 235 KB

The cyclisation of pyridine radicals derived from 2-bromo-N-alkyl pyridinium salts is described. The subsequent hydrogenation of the pyridinium salts is shown to give both the indolizidine and quinolizidine skeletons.