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January 25, 2026Organic & Biomolecular Chemistry0 citations

Enantioselective Michael additions promoted by a bifunctional charge-activated thiourea catalyst

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JNJosiah NislySKSteven R. Kass

Key Points

  • The aim is to synthesize a new bifunctional thiourea catalyst and evaluate its enantioselective activity.
  • Development of a new bifunctional thiourea catalyst with a methylated pyridinium ion and chiral amine.
  • Comparison of catalytic activity against Takemoto's catalyst in Michael addition reactions.
  • The new organocatalyst shows increased activity compared to analogous thiourea catalysts.
  • Significant improvement in enantioselectivity observed during Michael addition reactions.

Abstract

A new bifunctional thiourea featuring a methylated pyridinium ion and a chiral amine is reported. This readily prepared organocatalyst is more active than its analogous 3,5bis(trifluoromethyl)phenyl substituted thiourea ("Takemoto's catalyst"),...

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Cite This Study

Nisly et al. (2025) studied this question.

synapsesocial.com/papers/6975b1a9feba4585c2d6d1e5https://doi.org/10.1039/d5ob01845e
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