Chiral synthons from carvone. Part 53. First enantiospecific synthesis of (-)-9-pupukeanone
| Data(s) |
04/02/2002
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| Resumo |
The first enantiospecific total synthesis of (-)-9-pupukeanone, starting from (R)-carvone employing a combination of Michael-Michael reaction and an intramolecular rhodium carbenoid C H insertion reaction as key steps, is described. (C) 2002 Elsevier Science Ltd. All rights reserved. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/39047/1/First_enantiospecific.pdf Srikrishna, A and Kumar, Ravi P (2002) Chiral synthons from carvone. Part 53. First enantiospecific synthesis of (-)-9-pupukeanone. In: Tetrahedron Letters, 43 (6). pp. 1109-1111. |
| Publicador |
Elsevier Science |
| Relação |
http://dx.doi.org/10.1016/S0040-4039(01)02336-X http://eprints.iisc.ernet.in/39047/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
