Maity, Soumitra ; Ghosh, Subrata (2009) A direct route to angularly substituted hydrindanes. Formal synthesis of bakkenolide-A and synthesis of an advanced intermediate to umbellactal Tetrahedron, 65 (45). pp. 9202-9210. ISSN 0040-4020
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...
Related URL: http://dx.doi.org/10.1016/j.tet.2009.09.029
Abstract
A direct route for the synthesis of highly functionalized angularly substituted hydrindanes has been developed. The key step involves RO-RCM of an appropriately functionalized norbornene derivative. The hydrindane derivative obtained in this way has been used to accomplish a formal synthesis of bakkenolide-A. This protocol has also been extended for the synthesis of an advanced intermediate to the synthesis of the diterpene umbellactal.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
Keywords: | Hydrindanes; Metathesis; Spiro Lactones; Terpenes |
ID Code: | 12380 |
Deposited On: | 10 Nov 2010 06:19 |
Last Modified: | 12 Feb 2011 10:36 |
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