Saturated heterocycles, 176. Synthesis and steric structure of quaternary azeto[2,1-A]isoquinoline stereoisomers
Starting from l-substituted azeto[2,1-a]isoquinoline diastereomers, a number of quaternary salts were prepared. The reactions leading to the quaternary salts were stereospecific, independently of the configuration at C-l, resulting in diastereomers. The steric structures of the new compounds were pr...
Elmentve itt :
| Szerzők: | |
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| Dokumentumtípus: | Cikk |
| Megjelent: |
1991
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| Sorozat: | JOURNAL OF HETEROCYCLIC CHEMISTRY
28 |
| Tárgyszavak: | |
| doi: | 10.1002/jhet.5570280228 |
| mtmt: | 28033 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/32323 |
| Tartalmi kivonat: | Starting from l-substituted azeto[2,1-a]isoquinoline diastereomers, a number of quaternary salts were prepared. The reactions leading to the quaternary salts were stereospecific, independently of the configuration at C-l, resulting in diastereomers. The steric structures of the new compounds were proved by nmr spectroscopy. |
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| Terjedelem/Fizikai jellemzők: | 353-357 |
| ISSN: | 0022-152X |