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II-oxo analogue irciniastatin B was also isolated.
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33645412735
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note
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The published spectral data, acquired in different NMR solvents, were insufficient to decisively establish a homomeric or diastereomeric correspondence between the two natural products.
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4
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0034571687
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Mulzer, J., Bohlmann, R., Eds.; Ernst Schering Research Foundation Workshop 32; Springer: New York
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(a) For a review, see: Narquizian, R.; Kocienski, P. J. In The Role of Natural products in Drug Discovery; Mulzer, J., Bohlmann, R., Eds.; Ernst Schering Research Foundation Workshop 32; Springer: New York, 2000; pp 25-56.
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Narquizian, R.1
Kocienski, P.J.2
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33645389846
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note
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(b) For a complete listing of structures of pederin related natural products including references, see the Supporting Information of ref 2.
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6
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0034618262
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For selected examples of total syntheses, see ref 4a and: (a) Kocienski, P.; Narquizian, R.; Raubo, P.; Smith, C.; Farrugia, L. J.; Muir, K.; Boyle, F. T. J. Chem. Soc., Perkin Trans. 1 2000, 2357.
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Smith, C.4
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Boyle, F.T.7
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12
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33645391227
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note
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Without exception, all ∼35 members of the pederin family display an identical cyclic left half pederate side chain; none of them display a dihydroisocoumarin unit in the bottom half.
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13
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22244436600
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During review of this manuscript, the synthesis and configuration of syn and anti models of the psymberin side chain was reported: Kiren, S.; Williams, L. J. Org. Lett. 2005, 7, 2905.
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(a) Kamila, S.; Mukherjee, C.; Mondal, S. S.; De, A. Tetrahedron 2003, 59, 1339.
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Takahashi, H.1
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Kobayashi, S.5
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24
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33645389027
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note
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18
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25
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33645388100
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note
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See the Supporting Information.
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29
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33645390768
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note
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This approach has been used for the synthesis of pederin; see refs 4a and 5c and references therein.
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30
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33645406467
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note
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We thank Profs. Cherry Herald and George Pettit for kindly providing NMR spectra of irciniastatin A.
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