Alternative conditions for the synthesis of novel spiro[1,3-N,N-heterocyclic-adamantanes]
A series of new spiro[N-heterocyclic-adamantanes] was synthesized through the reaction of 2-adamantanone with beta-amino carboxamides. Depending on the chemical and physical characteristics of the starting compounds, the cyclocondensations proceeded under simple and mild (aqueous, solvent-free, ball...
Elmentve itt :
| Szerzők: | |
|---|---|
| Dokumentumtípus: | Cikk |
| Megjelent: |
Arkat U.S.A. Inc.
2015
|
| Sorozat: | ARKIVOC
2015 No. 7 |
| Tárgyszavak: | |
| doi: | 10.3998/ark.5550190.p009.268 |
| mtmt: | 2995982 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/5999 |
| Tartalmi kivonat: | A series of new spiro[N-heterocyclic-adamantanes] was synthesized through the reaction of 2-adamantanone with beta-amino carboxamides. Depending on the chemical and physical characteristics of the starting compounds, the cyclocondensations proceeded under simple and mild (aqueous, solvent-free, ball-milling or/and microwave-assisted) conditions with no necessity for chromatographic purification of the products. The reaction was extended to leucinamide and salicylamide. |
|---|---|
| Terjedelem/Fizikai jellemzők: | 158-171 |
| ISSN: | 1551-7004 |