1H and13C NMR spectra, stereoisomerism, and conformational states of 3-phenyl-5-isopropoxytetrahydro-2-furanones
✍ Scribed by A. A. Panasenko; A. A. Fatykhov; L. V. Spirikhin; G. A. Tolstikov
- Publisher
- Springer US
- Year
- 1988
- Tongue
- English
- Weight
- 341 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0009-3122
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## Abstract The ^1^H and ^13^C NMR resonances of thirty 2‐functionalized 5‐(methylsulfonyl)‐1‐phenyl‐1__H__‐indoles were assigned completely and unequivocally using the concerted application of one‐ and two‐dimensional experiments (DEPT, gs‐HMQC and gs‐HMBC). Finally, the influence of the 2‐substit
A set of 3-alkylaminoacroleins (R1NHCHxCHCHxO, R1 \ alkyl) were studied by 13C and 1H NMR spectroscopy in solutions of di †erent solvents and, for the simplest representative of the series, 3methylaminoacrolein, at di †erent temperatures. The equilibrium solutions of these compounds consists of mixt