Sunnam, Sunil Kumar ; Prasad, Kavirayani R. (2014) Enantioselective synthesis of macrolactone core of the natural product Sch725674 Tetrahedron, 70 (12). pp. 2096-2101. ISSN 0040-4020
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tet.2014.02.008
Abstract
An enantioselective synthesis of the macrolactone core of natural product Sch725674 was accomplished from furfural. Key reactions in assembly of the macrolactone are the use of furan as a but-2-ene-dione equivalent and ring closing metathesis.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Macrolide; Total Synthesis; Natural Products; Sch725674 |
| ID Code: | 105630 |
| Deposited On: | 21 Dec 2017 12:04 |
| Last Modified: | 21 Dec 2017 12:04 |
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