Hydrogen Bond‐Assisted Macrocyclic Synthesis: An Extended Application For 4‐Hydroxybenzylamine Derivatives

Abstract This work involved synthesizing three N ‐benzyl‐4‐hydroxybenzylamines using indirect reductive amination of aromatic aldehydes and 4‐hydroxybenzylamine. Such benzylamines’ reaction with formaldehyde produced tricyclic azacyclophanes formed by two benzylamine units joined by methylene bridges. Computational calculations established that macrocyclization was promoted by template formation stabilized by hydrogen bonds and π‐stacking.

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Journal
ChemistrySelect
Published
2024-09-09
DOI
https://doi.org/10.1002/slct.202402715
Citations
1
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.23
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Hydrogen Bond‐Assisted Macrocyclic Synthesis: An Extended Application For 4‐Hydroxybenzylamine Derivatives

Rodolfo Quevedo, Andrés Gonzalez‐Oñate, Jorge Alí‐Torres
1 citations
ChemistrySelect
Chemical Synthesis and Analysis
0.23
article

Hydrogen Bond‐Assisted Macrocyclic Synthesis: An Extended Application For 4‐Hydroxybenzylamine Derivatives

Rodolfo Quevedo, Andrés Gonzalez‐Oñate, Jorge Alí‐Torres
article en
1 citations

Abstract

Abstract This work involved synthesizing three N ‐benzyl‐4‐hydroxybenzylamines using indirect reductive amination of aromatic aldehydes and 4‐hydroxybenzylamine. Such benzylamines’ reaction with formaldehyde produced tricyclic azacyclophanes formed by two benzylamine units joined by methylene bridges. Computational calculations established that macrocyclization was promoted by template formation stabilized by hydrogen bonds and π‐stacking.

ChemistrySelectVol. 9(34)
Universidad Nacional de Colombia (CO)
Clean water and sanitation
Openalex Percentile: Top 43%
Chemical Synthesis and Analysis
0.23
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