130248-77-0Relevant academic research and scientific papers
Catalytic asymmetric synthesis of 1,3-enyne scaffolds: Design and synthesis of conjugated nitro dienynes as novel Michael acceptors and development of a new synthetic methodology
Li, Xiang,Peng, Fangzhi,Zhou, Mingtao,Mo, Mingjie,Zhao, Ruirui,Shao, Zhihui
, p. 1745 - 1747 (2014/02/14)
A novel catalytic enantioselective synthesis of functionalized 1,3-enynes has been developed featuring the design and synthesis of conjugated nitro dienynes as a useful new class of Michael acceptors. Moreover, a simple, yet flexible catalytic cascade approach to functionalized enantioenriched acyclic α,β-enones and cyclic dienones has also been developed.
A new synthesis of substituted fulvenes
Lee, Gary C. M.,Tobias, Brian,Holmes, Judy M.,Harcourt, Dale A.,Garst, Michael E.
, p. 9330 - 9336 (2007/10/02)
A new fulvene synthesis results from the palladium-catalyzed [2 + 2 + 2] annulation of 1 mol of a β-substituted vinyl iodide and 2 mol of a monosubstituted acetylene. This variant of the Heck reaction tolerates a wide range of substrate substituents with
