Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone
| Data(s) |
28/10/2010
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| Resumo |
The enantiospecific total synthesis of two epimers of the sesquiterpene isocalamusenone has been accomplished starting from the readily available monoterpene (R)-limonene which of the natural product established the stereostructure and the absolute configuration (C) 2010 Elsevier Ltd All rights reserved |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/35006/1/Total.pdf Srikrishna, Adusumilli and Pardeshi, Vijendra H and Mahesh, Konda (2010) Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone. In: Tetrahedron: Asymmetry, 21 (20). pp. 2512-2516. |
| Publicador |
Elsevier Science |
| Relação |
http://dx.doi.org/10.1016/j.tetasy.2010.09.008 http://eprints.iisc.ernet.in/35006/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
