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In press
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Synthesis of the chiral silane reagents: Beresis, R. T.; Solomon, J. S.; Yang, M. J.; Jain, N. F.; Panek, J. S. Org. Synth. In press.
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16944363905
-
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note
-
4/S, all of which resulted in complex mixtures.
-
-
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-
25
-
-
16944364907
-
-
note
-
13C NMR, IR, MS, and HRMS spectral data.
-
-
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27
-
-
16944363664
-
-
note
-
4 is commercially available from Aldrich Chemical Co.
-
-
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28
-
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16944363720
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note
-
1H NMR of these substrates indicated substantial desilation and displayed a para-substituted splitting pattern of the aromatic protons.
-
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29
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84943392701
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0000403720
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The PhI=NTs was prepared according to Yamada et al. (Yamada, Y.; Yamamoto, T.; Okawara, M. Chem Lett. 1975, 361-362) with modifications as described in the Experimental Section.
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16944365636
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Commercially available from Aldrich Chemical Co.
-
Commercially available from Aldrich Chemical Co.
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44
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-
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16944366675
-
-
note
-
Proof of the absolute stereochemistry of the allylic N-tosylamines was obtained by correlation of the known allylic nitro compound 2a to the allylic N-tosylamine 7a via the following sequence: (see Supporting Information for experimental details).
-
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47
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16944367273
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16944362716
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See the Experimental Section for the preparation of silanes 6f and 6g
-
See the Experimental Section for the preparation of silanes 6f and 6g.
-
-
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51
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For an excellent and comprehensive review of substrate-directable reactions, see: Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307-1370.
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