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For relative stereochemistry and absolute configuration of sarcophytol B, see: Kobayashi, M.; Iesaka, T.; Nakano, E. Chem. Pharm. Bull. 1989, 37, 2053; for the synthetic studies on sarcophytol B, see: (a) McMurry, J. E.; Rico, J. G.; Shih, Y.-N.; Tetrahedron Lett. 1989, 30, 1173;
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13 by silylation(TBSCI, imidazole, DMF, 23 °C, 100%)
-
13 by silylation(TBSCI, imidazole, DMF, 23 °C, 100%).
-
-
-
-
34
-
-
0013517705
-
-
note
-
+, 1%).
-
-
-
-
35
-
-
0013558005
-
-
Authentic sample was not available for direct comparsion
-
Authentic sample was not available for direct comparsion.
-
-
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36
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0028835945
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1H NMR spectra according to Allevi, P.; Cajone, F.; Ciuffreda, P.; Anastasia, M. Tetrahedron Lett. 1995, 36, 1347.
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37
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0001290346
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For example, see: Heathcock, C. H.; Pirrung, M. C.; Young, S. D.; Hagen, J. P.; Jarvi, E. T.; Badertscher, U.; Marki, H.-P.; Montgomery, S. H. J. Am. Chem. Soc. 1984, 106, 8161.
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Marki, H.-P.7
Montgomery, S.H.8
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38
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0001510414
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For examples, see: (a) Lee, A. W. M.; Martin, V. S.; Masamune, S.; Sharpless, K. B.; Walker, F. J. J. Am. Chem. Soc. 1982, 104, 3515;
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41
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0013556920
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Financial support of this work was provided by the National Science Foundation of China (No. 29672015)
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Financial support of this work was provided by the National Science Foundation of China (No. 29672015).
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