Total synthesis of the marine alkaloid mansouramycin D
Total synthesis of the marine alkaloid mansouramycin D
| dc.contributor.author | Prakash, K. S. | |
| dc.contributor.author | Nagarajan, Rajagopal | |
| dc.date.accessioned | 2022-03-27T08:40:00Z | |
| dc.date.available | 2022-03-27T08:40:00Z | |
| dc.date.issued | 2014-01-03 | |
| dc.description.abstract | Mansouramycin D, a cytotoxic alkaloid was isolated from a marine Streptomyces sp. in 2009. The first, simple, and concise route to the total synthesis of Mansouramycin D is reported. The core structure of the isoquinoline ring has been constructed from iminoannulation of 2-alkynylbenzaldehyde followed by oxidation/deprotection and oxidative amination via a three-step sequence from easily accessible starting materials. © 2013 American Chemical Society. | |
| dc.identifier.citation | Organic Letters. v.16(1) | |
| dc.identifier.issn | 15237060 | |
| dc.identifier.uri | 10.1021/ol4032396 | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/ol4032396 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/11424 | |
| dc.title | Total synthesis of the marine alkaloid mansouramycin D | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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