Chiral synthons from campholenaldehyde: enantiospecific synthesis of diquinane and linear triquinanes
Data(s) |
08/09/2010
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Resumo |
Enantiospecific syntheses of diquinane and linear triquinanes were accomplished, starting from the readily available alpha-campholenaldehyde employing a Nazarov reaction as the key step. (C) 2010 Elsevier Ltd. All rights reserved. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/33399/1/chiral.pdf Srikrishna, Adusumilli and Neetu, Ghodke (2010) Chiral synthons from campholenaldehyde: enantiospecific synthesis of diquinane and linear triquinanes. In: Tetrahedron: Asymmetry, 21 (17). pp. 2067-2071. |
Publicador |
Elsevier Science |
Relação |
http://dx.doi.org/10.1016/j.tetasy.2010.06.020 http://eprints.iisc.ernet.in/33399/ |
Palavras-Chave | #Organic Chemistry |
Tipo |
Journal Article PeerReviewed |