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For other approaches to the carbocyclic system of 1, see: Whitesell, J. K.; Minton, M. A. J. Am. Chem. Soc. 1987, 109, 6403 and references therein
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Boeckman, R. K. Jr.; Napier, J. J.; Thomas, E. W.; Sato, R. I. J. Org. Chem. 1983, 48, 4152. For other approaches to the carbocyclic system of 1, see: Whitesell, J. K.; Minton, M. A. J. Am. Chem. Soc. 1987, 109, 6403 and references therein.
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0022899041
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For a discussion of the various synthetic strategies for formation of the macrocyclic ring, see: Boeckman, R. K., Jr.; Perni, R. B. J. Org. Chem. 1986, 51, 5486.
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0024451471
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See the following paper in this issue for an alternative total synthesis of (+)-1 by Paquette and co-workers
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following paper in this issue
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See the following paper in this issue for an alternative total synthesis of (+)-1 by Paquette and co-workers: Paquette, L. A.; Macdonald, D.; Anderson, L.; Wright, J. J. Am. Chem. Soc. 1989, 111, following paper in this issue.
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Paquette, L.A.1
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Use of highly electrophilic oxidants was precluded by the unexpectedly high reactivity of the strained double bond in 2
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Moriarity, R. M.; Hou, K. C. Tetrahedron Lett. 1984, 25, 691. Use of highly electrophilic oxidants was precluded by the unexpectedly high reactivity of the strained double bond in 2.
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For an example of a similar epimerization, see: Corey, E. J.; Wollenberg, R. H. J. Org. Chem. 1975, 40, 2265.
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