Enantiospecific synthesis of pacifigorgianes
Data(s) |
01/02/2012
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Resumo |
Enantiospecific synthesis of the sesquiterpenes pacifigorgianes has been described. (R)-Carvone has been employed as the chiral starting material and an entropy assisted ring-closing metathesis reaction by Grubbs first generation catalyst was employed as the key strategy. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/44092/1/Enantiospecific.pdf Srikrishna, A and Dethe, Dattatraya H (2012) Enantiospecific synthesis of pacifigorgianes. In: Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry, 51 (2). pp. 345-355. |
Publicador |
National Institute of Science Communication and Information Resources |
Relação |
http://nopr.niscair.res.in/handle/123456789/13574 http://eprints.iisc.ernet.in/44092/ |
Palavras-Chave | #Organic Chemistry |
Tipo |
Journal Article PeerReviewed |