## Abstract Carbon‐13 NMR chemical shifts and carbon‐proton coupling constants for nine 4‐substituted and six 5‐substituted pyrimidines are reported. The carbon chemical shifts are correlated with π‐electron densities. Carbon‐proton coupling constants fail to correlate with substituent electronegat
Proton and carbon-13 NMR spectra of some 3,4-fused pyranocoumarins and furocoumarins
✍ Scribed by Amarendra Patra; Samir K. Panda; K. C. Majumdar; A. T. Khan; S. Saha
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 290 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Carbon-1 3 spectral assignments of five pyrano[3,2-c] [l]benzopyran-5(2H) -ones, five pyrano[2,3-c] [l ]benzopyran-5(2H)ones and five 2-methylfuro[2,3-c] [ l ] benzopyran-4-ones and of 2-methylfuro[3, 2-c] [l]benzopyran-4-one and 4-(2-chloroallyl)-3-hydroxycoumarin were made from mutual correlations, 13C/' H coupling constant measurements and 2D X-H correlation analyses. High-resolution proton resonance assignments of these compounds are reported.
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