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For recent examples see: (a) Bennett, S.M.W.; Brown, S.M.; Muxworthy, J.P.; Woodward, S. Tetrahedron Lett. 1999, 40, 1767-1770;
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Tetrahedron Lett.
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Bennett, S.M.W.1
Brown, S.M.2
Muxworthy, J.P.3
Woodward, S.4
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7
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(b) Kanai, M.; Nakagawa, Y.; Tomioka, K. Tetrahedron 1999, 55, 3831-3842;
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Kanai, M.1
Nakagawa, Y.2
Tomioka, K.3
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8
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0032558607
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(c) Alexakis, A.; Vastra, J.; Burton, C.; Benhaim, C.; Mangeney, P. Tetrahedron Lett. 1998, 39, 7869-7872.
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Alexakis, A.1
Vastra, J.2
Burton, C.3
Benhaim, C.4
Mangeney, P.5
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9
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4243489506
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For a review of functionalized zinc reagents, see: Knochel, P.; Singer, R.D. Chem. Rev. 1993, 93, 2117-2188.
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Knochel, P.1
Singer, R.D.2
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10
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0030477791
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(a) de Vries, A.H.M.; Meetsma, A.; Feringa, B.L. Angew. Chem. Int. Ed. Engl. 1996, 35, 2374-2376;
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De Vries, A.H.M.1
Meetsma, A.2
Feringa, B.L.3
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11
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0031573812
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(b) Feringa, B.L.; Pineschi, M. Arnold, L.A. Imbos, R.; de Vries, A.H.M. Angew. Chem. Int. Ed. Engl.1997, 36, 2620-2623;
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Feringa, B.L.1
Pineschi, M.2
Arnold, L.A.3
Imbos, R.4
De Vries, A.H.M.5
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12
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0033540709
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(c) Naasz, R, Arnold, L.A. Pineschi, M.; Keller, E.; Feringa, B.L. J. Am. Chem. Soc. 1999, 121, 1104-1105.
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Naasz, R.1
Arnold, L.A.2
Pineschi, M.3
Keller, E.4
Feringa, B.L.5
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16
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0002831079
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Seebach, D.; Colvin, E.W.; Lehr, F.; Weller, T. Chimia 1979, 33, 1-18.
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Seebach, D.1
Colvin, E.W.2
Lehr, F.3
Weller, T.4
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20
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0030669550
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Keller, E.; Veldman, N.; Spek, A.L.; Feringa, B.L. Tetrahedron: Asymmetry 1997, 8, 3403-3413.
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Keller, E.1
Veldman, N.2
Spek, A.L.3
Feringa, B.L.4
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21
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0001346535
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Fornicola, R.S.; Oblinger, E.; Montgomery, J. J. Org. Chem. 1998, 63, 3528-3529.
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Fornicola, R.S.1
Oblinger, E.2
Montgomery, J.3
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24
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0009570133
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note
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Note that the α-position with respect to the ester and nitro groups is prone to epimerization.
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-
-
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26
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0009619206
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note
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3 was hampered by product decomposition. Analytically pure 7a and 7b were obtained by crystallization.
-
-
-
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27
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0009582572
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note
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13C NMR and by HRMS.
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