96547-44-3Relevant articles and documents
Copper-Catalyzed Silylcupration of Activated Alkynes
Vercruysse, Sébastien,Jouvin, Kévin,Riant, Olivier,Evano, Gwilherm
, p. 3373 - 3381 (2016/09/12)
A highly efficient catalytic silylcupration of activated alkynes is reported. Upon reaction with silylboronates and methanol in THF at room temperature in the presence of copper(I) fluoride tris(triphenylphosphine), a range of ynamides and propiolates were found to undergo a smooth silylcupration. This reaction, which tolerates various functional groups, affords a straightforward and efficient entry to the corresponding β-silylenamides and -acrylates, which were formed with high levels of regio- and stereoselectivities.
Stereochemistry of 3-oxo-5-phenylcyclo-pentanecarboxylic acids, XI: Syntheses of stereomeric 3-oxo-5-pyridylcyclopentanecarboxylic acids
Beck,Frahm
, p. 366 - 372 (2007/10/02)
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