1245286-42-3Relevant academic research and scientific papers
Enantioselective synthesis of (Z)-1,2-anti-2,5-anti-triol monosilyl ethers using a cross-metathesis allylboration sequence
Winbush, Susann M.,Roush, William R.
supporting information; experimental part, p. 4344 - 4347 (2010/11/18)
Figure Presented. The enantioselective synthesis of (Z)-1,2-anti-2,5-anti- triol monosilyl ethers via a two-step sequence involving olefin cross-metathesis of β-alkoxyallylboronate 4 and subsequent allylboration of the derived bisboryl intermediate 6 provides triol monoethers 7 with good to excellent diastereoselectivity.
