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2
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0013348681
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3
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0000512132
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4
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37049068802
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8
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Watanabe, H.1
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10
-
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1542404076
-
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This compound was prepared by PDC oxidation of 12 in 71% yield
-
This compound was prepared by PDC oxidation of 12 in 71% yield.
-
-
-
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11
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33845282886
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(a) Corey, E. J.; Bakshi, R. K.; Shibata, S. J. Am. Chem. Soc. 1987, 109, 5551.
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12
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33845282438
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(b) Corey, E. J.; Bakshi, R. K.; Shibata, S.; Chen, C.-P.; Singh, V. K. J. Am. Chem. Soc. 1987, 109, 7925.
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13
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0346267223
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(c) Mathre, D. J.; Jones, T. K.; Xavier, L. C.; Blacklock, T. J.; Reamer, R. A.; Mohan, J. J.; Tracy Turner Jones, E.; Hoogsteen, K.; Baum, M. W.; Grabowski, E. J. J. J. Org. Chem. 1991, 56, 751.
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Grabowski, E.J.10
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14
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0026035110
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(d) Jones, T. K.; Mohan, J. J.; Xavier, L. C.; Blacklock, T. J.; Mathre, D. J.; Sohar, P.; Tracy Turner Jones, E.; Reamer, R. A.; Roberts, F. E.; Grabowski, E. J. J. J. Org. Chem. 1991, 56, 763.
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Sohar, P.6
Tracy Turner Jones, E.7
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Roberts, F.E.9
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15
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0018631475
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Noyori, R.1
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16
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0000103208
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(b) Noyori, R.; Tomino, I.; Tanimoto, Y. J. Am. Chem. Soc. 1979, 101, 3129.
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17
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2142858450
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Enantiomeric excess of samples of 6 were determined by 400 MHz NMR analyses after converting to their MTPA esters. Absolute configuration of 6 was determined to be R by the modified Mosher method. See Ohtani, I.; Kusumi, T.; Kashman, Y.; Kakisawa, H. J. Am. Chem. Soc. 1991, 113, 4092.
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19
-
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1542508942
-
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The structures assigned to the respective new compounds were in accord with their IR, NMR, and MS spectra
-
The structures assigned to the respective new compounds were in accord with their IR, NMR, and MS spectra.
-
-
-
-
20
-
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1542718620
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-
note
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f0.37.
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22
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0000192963
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Oikawa, Y.1
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23
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33845559199
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24
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33746494993
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(a) Ito, Y.; Hirao, T.; Saegusa, T. J. Org. Chem. 1978, 43, 1011.
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Ito, Y.1
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0346541206
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(b) Minami, I.; Takahashi, K.; Shimizu, I.; Kimura, T.; Tsuji, J. Tetrahedron 1986, 42, 2971.
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Tsuji, J.5
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27
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0000650034
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(a) Miyashita, M.; Suzuki, T.; Yoshikoshi, A. Tetrahedron Lett. 1987, 28, 4293.
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0000037070
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(b) Miyashita, M.; Hoshino, M.; Yoshikoshi, A. Tetrahedron Lett. 1988, 29, 347.
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