Total synthesis of enokipodins A-D and cuparene-1,4-diol
| Data(s) |
01/10/2010
|
|---|---|
| Resumo |
A Claisen rearrangement and RCM reaction based sequence has been developed for total synthesis of the antifungal sesquiterpenes enokipodins A-D and cuparene-1,4-diol starting from 2,5-dimethoxy-4-methylhydroquinone. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/33842/1/Total.pdf Srikrishna, A and Rao, Srinivasa M (2010) Total synthesis of enokipodins A-D and cuparene-1,4-diol. In: Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry, 49 (10). pp. 1363-1371. |
| Publicador |
National Institute of Science Communication and Information Resources. |
| Relação |
http://nopr.niscair.res.in/handle/123456789/10395 http://eprints.iisc.ernet.in/33842/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
