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33750077116
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note
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For the synthesis of starting materials, reaction conditions for radical reactions, ee determination, and product stereochemical analysis, see Supporting Information.
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20
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7644235766
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(a) For a review on salen catalysts in synthesis, see: Cozzi, P. G. Chem. Soc. Rev. 2004, 33, 410.
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Cozzi, P.G.1
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(c) Taylor, M. S.; Zalatan, D. B.; Lerchner, A. M.; Jacobsen, E. N. J. Am. Chem. Soc. 2005, 127, 1313.
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Taylor, M.S.1
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23
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0037414319
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The relative stereochemistry was assigned by analogy of a very similar series of compounds. See: Yamashita, Y.; Saito, S.; Ishitani, H.; Kobayashi, S. J. Am. Chem. Soc. 2003, 125, 3793.
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Yamashita, Y.1
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24
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0037120883
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For site selectivity in radical addition to 2-methoxybenzoquinone, see: Ling, T.; Poupon, E.; Rueden, E. J.; Kim, S. H.; Theodorakis, E. A. J. Am. Chem. Soc. 2002, 124, 12261.
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0009476711
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Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: New York
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Rosenstein, I. J. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: New York, 2001; Vol. 1, pp 50-71.
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Rosenstein, I.J.1
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26
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33750059316
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note
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2 to the commercially available chloride catalyst.
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27
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33750052737
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note
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Tetraallyltin was found to be much more efficient than allyltributyltin.
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28
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13444265956
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Unni, A. K.; Takenaka, N.; Yamamoto, H.; Rawal, V. H. J. Am. Chem. Soc. 2005, 127, 1336.
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Unni, A.K.1
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29
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0037018443
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For a similar model, see: Huang, Y.; Iwama, T.; Rawal, V. H. Org. Lett. 2002, 4, 1163.
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Huang, Y.1
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Rawal, V.H.3
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