287483-41-4Relevant articles and documents
Sakurai reaction of 3,3-bis(silyl) silyl enol ethers with acetals involving selective desilylation of the geminal bis(silane). Concise synthesis of nematocidal oxylipid
Li, Linjie,Ye, Xincui,Wu, Ya,Gao, Lu,Song, Zhenlei,Yin, Zhiping,Xu, Yongjin
, p. 1068 - 1071 (2013/04/10)
3,3-Bis(silyl) silyl enol ethers have been shown to exhibit predominantly Sakurai reactivity, rather than Mukaiyama aldol reactivity, in their Lewis acid promoted reactions with acetals. Starting from a geminal bis(silyl) moiety consisting of two differen
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