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1
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0028239737
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Takahashi, C.; Takda, T.; Yamada, T.; Minoura, K.; Uchida, K.; Matsumura, E.; Numata, A. Tetrahedron Lett. 1994, 35, 5013.
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Tetrahedron Lett.
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Takahashi, C.1
Takda, T.2
Yamada, T.3
Minoura, K.4
Uchida, K.5
Matsumura, E.6
Numata, A.7
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2
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37049090785
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For strategies leading to this structural unit, see: (a) Thomas, E. J.; Whitehead, J. W. F. J. Chem. Soc., Perkin Trans. 1 1989, 507.
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(1989)
J. Chem. Soc., Perkin Trans.
, vol.1
, pp. 507
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Thomas, E.J.1
Whitehead, J.W.F.2
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3
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0026045019
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(b) Fisher, M. J.; Myers, C. D.; Joglar, J.; Chen, S-. H.; Danishefsky, S. J. J. Org. Chem. 1991, 56, 5826.
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J. Org. Chem.
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Fisher, M.J.1
Myers, C.D.2
Joglar, J.3
Chen, S.-.H.4
Danishefsky, S.J.5
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4
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0028240293
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Smith, A. B., III; Condon, S. M.; McCauley, J. A.; Leahy, J. W.; Leazer, J. L.; Maleczka, R. E. Tetrahedron Lett.. 1994, 35, 4907.
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(1994)
Tetrahedron Lett.
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, pp. 4907
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Smith A.B. III1
Condon, S.M.2
McCauley, J.A.3
Leahy, J.W.4
Leazer, J.L.5
Maleczka, R.E.6
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5
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0026551401
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Evans, D. A.; Miller, S. J.; Ennis, M. D.; Ornstein, P. L. J. Org. Chem. 1992, 57 1067.
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J. Org. Chem.
, vol.57
, pp. 1067
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Evans, D.A.1
Miller, S.J.2
Ennis, M.D.3
Ornstein, P.L.4
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6
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0000215820
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(e) Corey, E. J.; Weigel, L. O.; Chamberlin, A. R.; Lipshutz, B. J. Am. Chem. Soc. 1980, 102, 1439.
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(1980)
J. Am. Chem. Soc.
, vol.102
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Corey, E.J.1
Weigel, L.O.2
Chamberlin, A.R.3
Lipshutz, B.4
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7
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0342569442
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note
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13C (125 MHz) NMR spectra, as well as appropriate parent ion identification by high-resolution mass spectrometry.
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-
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8
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0029892482
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Available from Aldrich Chemical Company or for a recent preparative procedure, see: Babler, J. H.; Liptak, V. P.; Trautmann, J. A.; Zayia, G. H. Synth. Commun. 1996, 26, 1943.
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(1996)
Synth. Commun.
, vol.26
, pp. 1943
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Babler, J.H.1
Liptak, V.P.2
Trautmann, J.A.3
Zayia, G.H.4
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9
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0343439370
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(a) Zeller, P.; Bader, F.; Lindlar, H.; Montavon, M.; Muller, P.; Ruegg, R.; Ryser, G.; Saucy, G.; Schaeren, S. F.; Schwieter, U.; Stricker, K.; Tamm, R.; Zurcher, P.; Isler, O. Helv. Chim. Acta 1959, 42, 841.
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(1959)
Helv. Chim. Acta
, vol.42
, pp. 841
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Zeller, P.1
Bader, F.2
Lindlar, H.3
Montavon, M.4
Muller, P.5
Ruegg, R.6
Ryser, G.7
Saucy, G.8
Schaeren, S.F.9
Schwieter, U.10
Stricker, K.11
Tamm, R.12
Zurcher, P.13
Isler, O.14
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10
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84984084114
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(b) Ruegg, R.; Lindlar, H.; Montavon, M.; Saucy, G.; Schaeren, S. F.; Schweiter, U.; Isler, O. Helv. Chim. Acta 1959, 42, 847.
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(1959)
Helv. Chim. Acta
, vol.42
, pp. 847
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-
Ruegg, R.1
Lindlar, H.2
Montavon, M.3
Saucy, G.4
Schaeren, S.F.5
Schweiter, U.6
Isler, O.7
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12
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0000604671
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Heathcock has investigated 3-thiopropenals in stereoselective aldol reactions and reported that they can be selectively manipulated to produce either syn-or anti-aldol products, see: Danda, H.; Hansen, M. M.; Heathcock, C. H. J. Org. Chem. 1990, 55, 173.
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(1990)
J. Org. Chem.
, vol.55
, pp. 173
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Danda, H.1
Hansen, M.M.2
Heathcock, C.H.3
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13
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33845556160
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(a) Evans, D. A.; Nelson, J. V.; Vogel, E.; Taber, T. R. J. Am. Chem. Soc. 1981, 103, 3099.
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(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 3099
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Evans, D.A.1
Nelson, J.V.2
Vogel, E.3
Taber, T.R.4
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15
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0342569438
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note
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Given that the binary mixture is reduced to a single product upon reductive removal of the chiral auxiliary, this byproduct is likely derived from dehydration of the anti-or non-Evans syn aldol product.
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16
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0342569437
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Reference 2a
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For the synthesis of (+)-9, see: (a) Reference 2a.
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