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See, for example, Hirohara, H.; Mitsuda, S.; Audo, E.; Komaki, R. In Biocatalysts in Organic Synthesis; Tramper, J., Van der Plas, H. C., Linko, P., Eds.; Elsevier: Amsterdam, 1985; p 119. See also Johnson, C. R.; Barbachyn, M. J. Am. Chem. Soc. 1982, 104, 4290. Greuter, H.; Dingwall, J.; Martin, P.; Bellus, D. Helv. Chim. Acta 1981, 64, 2812. Kim, G.; Chu-Moyer, M. Y.; Danishefsky, S. J.; Schulte, G. K. J. Am. Chem. Soc. 1993, 115, 30. Salaün, J. Top. Curr. Chem. 2000, 207, 1. Pietruszka, J. Chem. Rev. 2003, 103, 1051. Wessjohann, L. A.; Brandt, W.; Thiemann, T. Chem. Rev. 2003, 103, 1625.
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The low stability of the benzyl derivatives 2c and 3c - they decomposed upon standing at room temperature for several hours - justified that their use in further transformations was discarded.
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2O (200 mg). The mixture was stirred overnight, filtered through a Celite pad, and concentrated under reduced pressure.
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62
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12344251105
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note
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All the tested chromatographic attempts to purify compounds 8a and 8b were unsuccessful.
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63
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note
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Chromatographic purification of these compounds was unsuccessful in our hands.
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