Mehta, Goverdhan ; Shinde, Harish M. (2005) Enantioselective total synthesis of bioactive natural product (+)- Sch 642305: a structurally novel inhibitor of bacterial DNA primase and HIV-1 Tat transactivation Chemical Communications (29). pp. 3703-3705. ISSN 1359-7345
![[img]](http://repository.ias.ac.in/style/images/fileicons/application_pdf.png)
|
PDF
- Publisher Version
260kB |
Official URL: http://pubs.rsc.org/en/Content/ArticleLanding/2005...
Related URL: http://dx.doi.org/10.1039/B505264E
Abstract
The total synthesis of the bioactive natural product (+)-Sch 642305 has been achieved from a readily available chiral building block using an RCM protocol to construct the key decalactone moiety; our approach is notable for its built-in flexibility and is diversity oriented.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Royal Society of Chemistry. |
| ID Code: | 29088 |
| Deposited On: | 18 Dec 2010 05:37 |
| Last Modified: | 17 May 2016 12:03 |
Repository Staff Only: item control page
