Mehta, Goverdhan ; Kundu, Uday Kumar (2005) Toward a total synthesis of the novel polyketide natural product spiculoic acid A Organic Letters, 7 (25). pp. 5569-5572. ISSN 1523-7060
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Official URL: http://pubs.acs.org/doi/abs/10.1021/ol0521329
Related URL: http://dx.doi.org/10.1021/ol0521329
Abstract
An enantioselective approach toward the recently isolated marine natural product, spiculoic acid A, conceptualized along the proposed biogenetic hypothesis, involving an intramolecular Diels-Alder reaction as the pivotal step, is delineated. Access to a structurally embellished bicyclic core of the natural product has been accomplished.
Item Type: | Article |
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Source: | Copyright of this article belongs to American Chemical Society. |
ID Code: | 28989 |
Deposited On: | 18 Dec 2010 05:44 |
Last Modified: | 18 Dec 2010 05:44 |
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