287483-50-5Relevant articles and documents
Asymmetric synthesis of the new marine epoxy lipid, (6S,7S,9S,10S)-6,9-epoxynonadec-18-ene-7,10-diol
Yoda, Hi Demi,Maruyama, Kazuhide,Takabe, Kunihiko
, p. 1403 - 1406 (2007/10/03)
An efficient and stereocontrolled process is described for the preparation of (6S,7S,9S,10S)-6,9-epoxynonadec-18-ene-7,10-diol, a marine epoxy lipid isolated from the brown alga, Notheia anomala. The key 2,3,5-trisubstituted tetrahydrofuran ring was const
Enantiocontrolled synthesis of C-19 tetrahydrofurans isolated from the marine alga Notheia anomala
García, Celina,Soler, Marcos A.,Martín, Víctor S.
, p. 4127 - 4130 (2007/10/03)
The stereocontrolled synthesis of (2S,3S,5R)-5-[(1R)-1-hydroxy-9- decenyl]-2-pentyltetrahydro-3-furanol and (2S,3S,5S)-5-[(1S)-1-hydroxy-9- decenyl]-2-pentyltetrahydro-3-furanol, both isolated from the brown alga Notheia anomala has been achieved. The req