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- W2004011617 abstract "The target antifungal molecule is an equipotent 1-cytosinyl analogue of natural Malayamycin A, its 3-cytosinyl congener. The synthesis relies solely on substrate control to introduce all six contiguous stereogenic centers. The key steps are (a) the ring-closing metathesis (RCM) reaction used to create the bicycle B and (b) the N-nucleosidation via activation of the O,S-acetal F." @default.
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- W2004011617 date "2006-09-01" @default.
- W2004011617 modified "2023-09-27" @default.
- W2004011617 title "Synthesis of 1-Cytosinyl-N-malayamycin A" @default.
- W2004011617 doi "https://doi.org/10.1055/s-2006-949317" @default.
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