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For the synthesis of citreoviral and citreoviridin in both racemic and optically active form, see: (a) Hanaki, N.; Link, J. T.; MacMillan, D. W. C.; Overman, L. E.; Trankle, W. G.; Wurster, J. A. Org. Lett. 2000, 2, 223-226.
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(h) Hatakeyama, S.; Matsui, Y.; Suzuki, M.; Sakurai, K.; Takano, S. Tetrahedron Lett. 1985, 26, 6485-6488.
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19
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For the synthesis of (+)-verrucosidin, see: (a) Hatakeyama, S.; Sakurai, K.; Numata, H.; Ochi, N.; Takano, S. J. Am. Chem. Soc. 1988, 110, 5201-5203.
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23
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For the applications of [3 + 2] annulation of allylic silanes in natural product synthesis, see, for example: (a) Peng, Z.-H., Woerpel, K. A. Org. Lett. 2001, 3, 675-678.
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0032827689
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Isaka, M.; Williard, P. G.; Nakamura, E. Bull. Chem. Soc. Jpn. 1999, 72, 2115-2116.
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Isaka, M.1
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Nakamura, E.3
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28
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0041869437
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note
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Raising the reaction temperature from -78 °C to room temperature led to the Sakurai product 25 completely: (equation presented)
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31
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0042871473
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note
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The reaction of allylic silane 26, the methyl analogue of 6, with ethyl pyruvate gave tetrahydrofuran 27 in 90% yield as a single diastereomer: (equation presented)
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35
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0041368669
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See Supporting Information
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See Supporting Information.
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36
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0028151120
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Akiyama, T.; Yasusa, T.; Ishikawa, K.; Ozaki, S. Tetrahedron Lett. 1994, 35, 8401-8404.
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Akiyama, T.1
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Ozaki, S.4
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