Synthetic study of aquayamycin. Part 1: Synthesis of 3-(phenylsulfonyl)phthalides possessing a β-C-olivoside
✍ Scribed by Takashi Matsumoto; Hiroki Yamaguchi; Toshiyuki Hamura; Mitsujiro Tanabe; Yokusu Kuriyama; Keisuke Suzuki
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 84 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
An efficient synthetic route to 3-(phenylsulfonyl)phthalides possessing a b-C-olivoside was developed by exploiting the regioselective [2+2] cycloaddition of benzyne with ketene silyl acetal. The compounds are useful in the total synthesis of the angucyclines, including aquayamycin.
📜 SIMILAR VOLUMES
Six novel H 2 O-soluble b-cyclodextrin derivatives containing a 1,2-benzisoselenazol-3(2H)-one moiety were synthesized by a convenient method in 25 ± 60% yield and characterized by MS, elemental analysis, IR, 1 H-NMR, and UV/VIS spectroscopy. The conformations of these b-cyclodextrin derivatives 1 ±