96575-55-2Relevant academic research and scientific papers
One-pot transformation of silyl enol ethers into 1,3-dienes: In situ generation of alkenyl nonaflates and subsequent Heck reactions - Scope and limitations
Lyapkalo, Ilya M.,Webel, Matthias,Reissig, Hans-Ulrich
, p. 3646 - 3658 (2007/10/03)
Palladium-catalysed reactions between methyl acrylate and the isolated alkenyl nonaflates 2a, 2d and 2e proceed without difficulties, furnishing the desired 1,3-dienes 3, 14 and 15 in good yields. The use of other alkenyl nonaflates and olefins in this Heck reaction was also examined. The main purpose of this study was the development of an in situ generation of the required alkenyl nonaflates 2 from the corresponding silyl enol ethers 1 and their one-pot transformation into 1,3-dienes. Thus, the previously described fluoride-promoted exchange of the trimethylsilyl substituent of typical enol ethers 1 for a nonafluorobutylsulfonyl group was directly combined with the palladium-catalysed coupling step. This sequence allowed the efficient transformation of a variety of silyl enol ethers 1 into highly substituted 1,3-dienes in a practical one-pot procedure. The scope and limitations, together with the chemo- and stereoselectivity, of this process are discussed. A particular intriguing example involves a one-pot synthesis of silyl enol ether 1j by means of a Diels-Alder reaction, subsequent nonaflation and a Heck reaction with tert-butyl acrylate, furnishing the highly functionalised 1,3-diene 30 in good overall yield. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
Palladium-Catalyzed Olefination of Vinyl Triflates
Scott, William J.,Pena, Michael R.,Swaerd, Katarina,Stoessel, Steven J.,Stille, J. K.
, p. 2302 - 2308 (2007/10/02)
The olefination of vinyl trifluoromethanesulfonates (triflates) takes place under mild reaction conditions in polar solvents to give high yields of conjugated dienes.The reaction of 4-tert-butylcyclohexenyl triflate with Michael acceptors in the presence
