Supporting Information
Supporting Information File 1: Table of reaction conditions for KA2; experimental procedures, characterization data and copies of 1H and 13C NMR spectra for all new compounds; copies of NOESY-1D, gCOSY, NOESY and cartesian coordinates of compound 36; Smiles codes, PCA and PMI data for compounds 3–39. | ||
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Cite the Following Article
Combination of multicomponent KA2 and Pauson–Khand reactions: short synthesis of spirocyclic pyrrolocyclopentenones
Riccardo Innocenti, Elena Lenci, Gloria Menchi and Andrea Trabocchi
Beilstein J. Org. Chem. 2020, 16, 200–211.
https://doi.org/10.3762/bjoc.16.23
How to Cite
Innocenti, R.; Lenci, E.; Menchi, G.; Trabocchi, A. Beilstein J. Org. Chem. 2020, 16, 200–211. doi:10.3762/bjoc.16.23
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- Pauze, M. P. Ph.D. Thesis, Sept 28, 2021.
- Zorba, L. P.; Vougioukalakis, G. C. The Ketone-Amine-Alkyne (KA2) coupling reaction: Transition metal-catalyzed synthesis of quaternary propargylamines. Coordination Chemistry Reviews 2021, 429, 213603. doi:10.1016/j.ccr.2020.213603
- Innocenti, R.; Lenci, E.; Trabocchi, A. Recent advances in copper-catalyzed imine-based multicomponent reactions. Tetrahedron Letters 2020, 61, 152083. doi:10.1016/j.tetlet.2020.152083
- Lenci, E.; Puglielli, R. B.; Bucaletti, E.; Innocenti, R.; Trabocchi, A. A Glucose-Derived α-Hydroxy Aldehyde for the Petasis Reaction: Facile Access to Polyfunctional δ-Amino Acids. European Journal of Organic Chemistry 2020, 2020, 4227–4234. doi:10.1002/ejoc.202000600