ExcerptThe crude aldehyde, tert-butyl-3-methoxy-5,5-dimethyl-7-oxo-heptanoate  was treated with pinacol E-1-trimethylsilyl-1-propene-3-boronate  in petroleum ether at room temperature to provide a 50% yield of the diastereomeric boronic esters, which were simultaneously cleaved to the alcohols and readily separated by flash chromatography.[...] View Full-Text
Scifeed alert for new publicationsNever miss any articles matching your research from any publisher
- Get alerts for new papers matching your research
- Find out the new papers from selected authors
- Updated daily for 49'000+ journals and 6000+ publishers
- Define your Scifeed now
Smith, D.A. tert-Butyl-3-methoxy-5,5-dimethyl-7-hydroxy-8-trimethylsilyl-9-decenoate. Molecules 1997, 2, M33.
Smith DA. tert-Butyl-3-methoxy-5,5-dimethyl-7-hydroxy-8-trimethylsilyl-9-decenoate. Molecules. 1997; 2(10):M33.Chicago/Turabian Style
Smith, Douglas A. 1997. "tert-Butyl-3-methoxy-5,5-dimethyl-7-hydroxy-8-trimethylsilyl-9-decenoate." Molecules 2, no. 10: M33.
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.