Mechanistic Insights into the Stepwise (4+2) Cycloaddition toward Chiral Fused Uracil Derivatives

Abstract: The mechanism of the previously reported stereoselective (4+2) cycloaddition of N‐protected 6‐methyluracil‐5‐carbaldehydes and (E)‐β‐nitrostyrenes catalyzed by Takemoto's tertiary amine/thiourea organocatalyst was explored, using density functional theory (DFT) calculations on a model representative reaction. The cyclization reaction, which afforded notable enantioenriched carbocycle‐fused uracils embedding three contiguous stereocenters, was here proven to be the result of a four‐step sequence comprising a key stereo‐defining Michael addition, followed by a completely diastereoselective intramolecular Henry reaction. Going beyond the hitherto reported activation modes, a complex and unprecedented network of hydrogen‐bonding interactions between the chiral catalyst and the reaction partners has been disclosed, in which the protonated tertiary amine and the thiourea moiety of the catalyst simultaneously activate both the electrophile and the nucleophile components. By applying the Energetic Span Model (ESM) to four competitive energetic profiles, we unveiled the most plausible reaction pathways best fitting the experimental data, with close correlation with the observed enantiomeric ratio of the product.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Mechanistic Insights into the Stepwise (4+2) Cycloaddition toward Chiral Fused Uracil Derivatives ; day:28 ; month:04 ; year:2023 ; extent:10
Advanced synthesis & catalysis ; (28.04.2023) (gesamt 10)

Creator
Marcantonio, Enrico
Zanardi, Franca
Curti, Claudio
Lombardo, Marco

DOI
10.1002/adsc.202300045
URN
urn:nbn:de:101:1-2023042815450794023393
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:45 AM CEST

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Associated

  • Marcantonio, Enrico
  • Zanardi, Franca
  • Curti, Claudio
  • Lombardo, Marco

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