A combined pathway for the synthesis of nitidine family alkaloids
| Author | Pallikonda G. |
| Author | Hsieh C.-Y. |
| Author | Su H.-L. |
| Author | Hsieh J.-C. |
| Available date | 2020-04-01T09:45:58Z |
| Publication Date | 2019 |
| Publication Name | Research on Chemical Intermediates |
| Resource | Scopus |
| ISSN | 9226168 |
| Abstract | Three related alkaloids, oxynitidine, nitidine and 5,6-dihydronitidine, have been afforded by the new synthetic protocols. In this approach, the Ni-catalyzed annulation reaction is indicated as the key step to construct the isoquinolinone core structure. The subsequent transformations lead to the target alkaloids. - 2019, Springer Nature B.V. |
| Sponsor | We thank the Ministry of Science and Technology of Taiwan (ROC) for the financial support of this research (MOST 107-2113-M-032-006) and the fellowship for Gangaram Pallikonda (MOST 107-2811-M-032-002). Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
| Language | en |
| Publisher | Springer Netherlands |
| Subject | 5, 6-Dihydronitidine Alkaloids Benzo[c]phenanthridine Nitidine Oxynitidine |
| Type | Article |
| Pagination | 5399-5407 |
| Issue Number | 11 |
| Volume Number | 45 |
Files in this item
| Files | Size | Format | View |
|---|---|---|---|
|
There are no files associated with this item. |
|||
This item appears in the following Collection(s)
-
Central Laboratories Unit Research [86 items ]