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.
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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.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to National Institute of Science Communication and Information Resources.|
|Keywords:||Pacifigorgianes;bicyclo[4.3.0]nonanes;carvone;entropy effect; ring-closing metathesis;enantiospecific synthesis|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||28 Mar 2012 06:01|
|Last Modified:||28 Mar 2012 06:01|
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