330800-50-5

Upstream product

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• 109-72-8 n-butyllithium 
• 104804-92-4 3-(2-phenylethyl)-2-cyclopentenone 
• 90878-19-6 phenethylmagnesium chloride 
• 22627-70-9 3-ethoxycyclopent-2-en-1-one 

Relevant academic research and scientific papers

Asymmetric 1,4-reductions of and 1,4-additions to enoates and related systems

One aspect of the present invention relates to methods for the transition-metal-catalyzed asymmetric 1,4-addition of a nucleophile, e.g., hydride, to cyclic and acyclic enoates and enones. In certain embodiments of the methods of the present invention, th

Dynamic kinetic resolution via asymmetric conjugate reduction: Enantio- and diastereoselective synthesis of 2,4-dialkyl cyclopentanones

Herein, we report the kinetic and the dynamic kinetic resolutions of racemic 3,5-dialkyl-2-cyclopenten-1-ones. Kinetic resolution, with good selectivity factors (25-52), was achieved by conjugate reduction with catalytic CuCl/NaOt-Bu/(S)-p-tol-BINAP and s