A convenient approach towards 2′-analogs of zoapatanol from d-glucose
✍ Scribed by Huib Ovaa; Gijs A van der Marel; Jacques H van Boom
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 94 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The protected 3-C-methyl-a-D-allofuranose derivative 6, readily accessible from D-glucose, could be transformed into a diene scaffold which underwent ring-closing metathesis (RCM) to give the functionalized oxepines 10a,b. Further elaboration of 10a,b provided the 2%-zoapatanol analogs 3-5.
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