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The by-product 12 was presumably formed from the thioacetate 11 by a competitive S-O acetyl migration process. For a related example see: Heap J.M., Owen L.N. J. Chem. Soc. (C). 707:1970.
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85031171478
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note
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++H).
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20
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85031169753
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note
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4,F=33.9 Hz, C-4).
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85031168986
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note
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4S: 278.0611.
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22
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85031162770
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note
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++1).
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23
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85031171289
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note
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++1).
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25
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85031169147
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note
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2. The tested compounds were added to the cells seeded in triplicates in the concentration range of 0.78-100 μM and incubated for 72 h.
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26
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0036260829
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For recent reviews see: Chen S.H. Curr. Med. Chem. 9:2002;899 Gumina G., Song G.Y., Chu C.K. FEMS Microbiol. Lett. 202:2001;9 Maury G. Antivir. Chem. Chemoth. 11:2000;165 Wang P., Hong J.H., Cooperwood J.S., Chu C.K. Antiviral Res. 40:1998;19.
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For recent reviews see: Chen S.H. Curr. Med. Chem. 9:2002;899 Gumina G., Song G.Y., Chu C.K. FEMS Microbiol. Lett. 202:2001;9 Maury G. Antivir. Chem. Chemoth. 11:2000;165 Wang P., Hong J.H., Cooperwood J.S., Chu C.K. Antiviral Res. 40:1998;19.
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Gumina, G.1
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For recent reviews see: Chen S.H. Curr. Med. Chem. 9:2002;899 Gumina G., Song G.Y., Chu C.K. FEMS Microbiol. Lett. 202:2001;9 Maury G. Antivir. Chem. Chemoth. 11:2000;165 Wang P., Hong J.H., Cooperwood J.S., Chu C.K. Antiviral Res. 40:1998;19.
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For recent reviews see: Chen S.H. Curr. Med. Chem. 9:2002;899 Gumina G., Song G.Y., Chu C.K. FEMS Microbiol. Lett. 202:2001;9 Maury G. Antivir. Chem. Chemoth. 11:2000;165 Wang P., Hong J.H., Cooperwood J.S., Chu C.K. Antiviral Res. 40:1998;19.
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