Linear models are developed to predict the 13C NMR chemical shifts of carbons in indole moieties based on a critical review. These models fill a gap in the spectral simulation database which is used to simulate the 13C NMR spectra of a wide range of organic compounds, illustrating that this is a via
13C nuclear magnetic resonance spectra of ethers and glycols
β Scribed by C. Konno; H. Hikino
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- French
- Weight
- 563 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ^13^C Nuclear magnetic resonance (NMR) spectra of atactic and syndiotacticβrich poly(methacrylonitrile) (PMAN) were determined. In addition, 2D (^1^Hβ^13^C COSY)COSY = COrrelated SpectroscopY. NMR spectra of Ξ±βmethyl and methylene regions of atactic PMAN were measured. Values of tetrad
## Abstract The ^13^C NMR spectra of several diterpenic derivatives having the podocarpane and cassane skeleton were recorded and interpreted. The most significant effects due to substituent orientation, B/C ring junction stereochemistry and conformational changes are briefly discussed.
## Abstract The ^13^C and ^19^F (when appropriate) chemical shifts of a variety of diβ, triβ and tetrasubstituted methanes of the type CH~2~XCOOEt (I), CHXYCOOEt (II) and CXYZCOOEt (III), where the substituents X, Y and Z are F, Br, OEt, OPh, SEt, SPh and NO~2~, were determined. The prediction of t