Mehta, Goverdhan ; Shah, Shailesh R. (1991) Total synthesis of cervinomycin A1-trimethyl ether and cervinomycin A2-methyl ether Tetrahedron Letters, 32 (38). pp. 5195-5198. ISSN 0040-4039
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...
Related URL: http://dx.doi.org/10.1016/S0040-4039(00)93465-8
Abstract
The heptacyclic framework of cervinomycin antibiotics has been constructed through a C+EFG → CEFG → CDEFG → ABCDEFG approach in which the photochemical generation of ring D was a key step.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Xanthone Antibiotics; Photocyclisation; Tetrahydrooxazolo-[3,2-b]benz(g)isoquinolone Formation |
| ID Code: | 29222 |
| Deposited On: | 17 Dec 2010 08:23 |
| Last Modified: | 17 Dec 2010 08:23 |
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