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3. (a) Buszek, K.R.; Sato, N.; Jeong, Y. J. Am. Chem. Soc. 1994, 116, 5510-5512.
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0028965619
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4. Bach, J.; Berenguer, R.; Garcia, J.; Villarrasa, J. Tetrahedron Lett. 1995, 36, 3425.
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49549138922
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85030268902
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note
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2), chromatography using EtOAc/hexanes failed to remove the 3-pinanol by-product.
-
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-
-
10
-
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85030275880
-
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note
-
8. The ee of the TBS-ethers 5 and 13 were determined by capillary GC (chiradex-β, 100 °C, isothermal).
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11
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33751552977
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9. Roush, W. R.; Hoong, L. K.; Palmer, M. A.; Park, J. C. J. Org. Chem. 1990, 55, 4109. Bergelson, L. D.; Shemyakin, M. M. Tetrahedron Lett. 1963, 19, 149.
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12
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0043112679
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9. Roush, W. R.; Hoong, L. K.; Palmer, M. A.; Park, J. C. J. Org. Chem. 1990, 55, 4109. Bergelson, L. D.; Shemyakin, M. M. Tetrahedron Lett. 1963, 19, 149.
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Bergelson, L.D.1
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13
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45949121556
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0011802915
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Keck, G.E.1
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-
15
-
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85030274461
-
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note
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13C NMR peak height averaged differences.
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16
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33845554773
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13. Masamune, S.; Lu, L. D. -L.; Jackson, W. P.; Kaiho, T.; Toyoda, T. J. Am. Chem. Soc. 1982, 104, 5523.
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0016843151
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16. Corey, E. J.; Nicolaou, K. C.; Melvin, L. S. Jr. J. Am. Chem. Soc. 1975, 97, 653.
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33845378280
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17. Boden, P. B.; Keck, G. E.; J. Org. Chem. 1985, 50, 2394. Keck, G. E. Murry, J. A. J. Org. Chem. 1991, 56, 6606.
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85030273909
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note
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5.
-
-
-
-
24
-
-
85030275594
-
-
note
-
19. The substrates were synthesized following a modified route starting with 1,7-heptane diol, similar in manner to hydroxy acid 3 shown in figure 1.
-
-
-
-
25
-
-
85030267958
-
-
note
-
20. No ion was observed in the Mx2 region of the mass spectrum.
-
-
-
-
26
-
-
0001551488
-
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2), was isolated by distillation (53 °C, 20 mmHg). Ikeda, N.; Arai, I.; Yamamoto, H. J. Am. Chem. Soc. 1986, 108, 483.
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Ikeda, N.1
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27
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33847801219
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2ZrHCl was prepared according to: Buchwald, S. L.; LaMaire, S. J.; Nielsen, R. B.; Watson, B. T.; King, M. Tetrahedron Lett. 1987, 28, 3895.
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Hart, D.W.1
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-
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0001209154
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2ZrHCl was prepared according to: Buchwald, S. L.; LaMaire, S. J.; Nielsen, R. B.; Watson, B. T.; King, M. Tetrahedron Lett. 1987, 28, 3895.
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