Total synthesis of (-)-ent-pachastrissamine (ent-Jaspine B)
| Data(s) |
15/07/2011
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| Resumo |
The total synthesis of the enantiomer of the tetrahydrofuran containing natural product Jaspine B is reported. The key reactions in the synthesis include formation of the tetrahydrofuran unit by an acid mediated Williamson etherification and a subsequent elaboration with an olefin cross metathesis reaction. (C) 2011 Elsevier Ltd. All rights reserved. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/42102/1/total.pdf Prasad, Kavirayani R and Penchalaiah, Kamala (2011) Total synthesis of (-)-ent-pachastrissamine (ent-Jaspine B). In: Tetrahedron: Asymmetry, 22 (13). pp. 1400-1403. |
| Publicador |
Elsevier Science |
| Relação |
http://dx.doi.org/10.1016/j.tetasy.2011.07.010 http://eprints.iisc.ernet.in/42102/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
