Abstract
The novel heterocycles 1,11-dimethoxy-2-hydroxy-6-rnethyloxazolo[4,5-k]-5,6,6a,7-tetrahydro-4H-dibenzo [de,g]quinoline, 1,12-dimethoxy-2-hydroxy-6-methyl-9-phenyl-10H-oxazin[5,6-k]-5,6,6a,7- tetrahydro-4H-dibenzo[de,g]quinolin-10-one and 1,11-dimethoxy-2-hydroxy-6-methyl-9-phenyloxazolo[4,5-k]-5,6,6a,7-tetrahydro-4H- dibenzo[de,g]quinoline were prepared starting from the alkaloid boldine. The structures were confirmed and the 1H and 13C NMR spectra were completely assigned using a combination of one- and two-dimensional NMR techniques.
| Original language | English |
|---|---|
| Pages (from-to) | 361-366 |
| Number of pages | 6 |
| Journal | Magnetic Resonance in Chemistry |
| Volume | 39 |
| Issue number | 6 |
| DOIs | |
| State | Published - 2001 |
| Externally published | Yes |
Keywords
- C NMR
- H NMR
- Boldine
- NMR
- Oxazinone/aporphine derivatives
- Oxazolo/aporphine derivatives
Fingerprint
Dive into the research topics of 'Oxazine- and oxazole-fused derivatives of the alkaloid boldine and their complete structural and spectral assignments by HMQC and HMBC experiments'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver