𝔖 Bobbio Scriptorium
✦   LIBER   ✦

NMR study of organosilicon compounds. III—Silicon-29, nitrogen-14, carbon-13 and proton NMR spectra of silylakylamines

✍ Scribed by J. Schraml; Nguyen-Duc-Chuy; V. Chvalovský; M. Mägi; E. Lippmaa

Publisher
John Wiley and Sons
Year
1975
Tongue
English
Weight
773 KB
Volume
7
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Silicon-29 and carbon-13 NMR studies of
Silicon-29 and carbon-13 NMR studies of organosilicon chemistry. II—The Methylethoxysilanes MenSi(OEt)4−n
✍ Robin K. Harris; Barry J. Kimber 📂 Article 📅 1975 🏛 John Wiley and Sons 🌐 English ⚖ 555 KB

## Abstract Silicon‐29, carbon‐13 and oxygen‐17 NMR data are reported for the methylethoxysilanes, Me~__n__~Si(OEt)~4−__n__~ with __n__ = C to 3. The values of ^1^__J__(SiC) vary greatly, in a manner which appears to be inconsistent with an effect of __s__‐character variation alone. The chemical sh

Carbon-13 NMR studies of nitrogen compou
Carbon-13 NMR studies of nitrogen compounds. I—substituent effects of amino, acetamido, diacetamido, ammonium and trimethylammonium groups
✍ Jeanine Llinarés; José Elguero; Robert Faure; Emile-Jean Vincent 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 338 KB

## Abstract ^13^C NMR chemical shifts are reported for several alkyl or aryl amines, acetamides, diacetamides and ammonium and trimethylammonium salts. Substituent effects, determined with respect to chemical shifts of amino derivatives, are rationalized in terms of γ effects, steric interactions a

Carbon-13 NMR studies in the polycyclic
Carbon-13 NMR studies in the polycyclic hydrocarbon series. A new method for the identification of carbons α to a carbonyl group. Complete assignment of the 13C NMR spectra of several cis-decalins, cis-decalones, cis-hydrindanones and 13α,14α- and 13β,14β-steroids
✍ J. C. Gramain; J. C. Quirion 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 711 KB

A new 13C N M R method based on solvent effects allows the identification of carbon atoms a to a carbonyl group. With a simple change in solvent from CDCl, to CDC1,-dioxane (1:4), the -C absorption for all carbons except those a to the carbonyl group in the compounds under study were displaced to lo

Proton magnetic resonance studies of com
Proton magnetic resonance studies of compounds with bridgehead nitrogen atoms—XX: The NMR spectra and stereochemistry of some hexahydropyrido[2, 1-c] [1, 4] oxazin-3(4H)-ones and related compounds
✍ R. Cahill; T. A. Crabb 📂 Article 📅 1972 🏛 John Wiley and Sons 🌐 English ⚖ 779 KB

## Abstract A series of substituted hexahydropyrido [2,1‐__c__] [1,4] oxazin‐3(4__H__)‐ones has been synthesised, and the configurations of these bicyclic lactones assigned utilising chemical and spectral data. All the compounds adopt __trans__‐fused conformations and the conformation of the lacton