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note
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1. Postdoctoral Research associate on a grant from the U.S. Office of Naval Research.
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2
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0000584420
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Morrison J. D. Ed. Academic Press, Orlando, FL
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2. For reviews on the aldol reactions, see: (a) Heathcock, C. H. in Asymmetric Synthesis Vol.3, pp111-212., Morrison J. D. Ed. Academic Press, Orlando, FL, 1983
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Heathcock, C.H.1
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(b) Evans, D. A.; Nelson, J. V.; Taber, T. R.; Top. Stereochem. 1982, 13, 1-113.
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8
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(c) Evans, D. A.; Vogel, E.; Nelson, J. V. J. Am. Chem. Soc. 1979, 101, 6120.
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(e) Brown, H. C.; Dhar, R. K.; Bakshi, R. K.; Pandiarajan, P. K.; Singaram, B. J. Am. Chem. Soc. 1989, 111, 3441.
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(b) Evans, D. A.; Bartoli, J.; Shih, T. L. ibid. 1981, 103, 3099.
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(c) Masamune, S.; Choy, W.; Kerdesky, F. A.; Imperiali, B. J. Am. Chem. 1981, 103, 1566.
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(e) Bernardi, A.; Gennari, C.; Goodman, J. M.; Paterson, I. Tetrahedron: Asym. 1995, 6, 2613.
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13. Brown, H. C.; Chandrasekharan, J.; Ramachandran, P. V. J. Am. Chem. Soc. 1988, 110, 1539. DIP-Chloride™ is the Trade Mark of the Aldrich Chemical Company.
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note
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15. The poor ee produced in the aldol reaction of diisopinocampheylborinates of ethyl ketones with isobutyraldehyde led Paterson to believe that these "procedures are best suited to reactions with sterically undemanding aldehydes, i.e. α-branched saturated aldehydes should be avoided", Ref. 10a.
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