Synthesis of morpholine derivatives from 1,3-dienes and N-arylaminoalcohols by palladium-catalyzed sequential C–N and C–O bond formation

Abstract

We developed a palladium-catalyzed oxidative coupling of 1,3-dienes with N-arylaminoalcohols to synthesize morpholine derivatives. Using a copper salt and 1,4-benzoquinone with molecular oxygen afforded high yields. DFT calculations elucidated the chemical selectivity and revealed that 1,4-benzoquinone acts as a ligand promoting reductive elimination, offering mechanistic insight into the catalytic cycle.

Graphical abstract: Synthesis of morpholine derivatives from 1,3-dienes and N-arylaminoalcohols by palladium-catalyzed sequential C–N and C–O bond formation

Supplementary files

Article information

Article type
Communication
Submitted
06 Nov 2025
Accepted
16 Dec 2025
First published
17 Dec 2025

Org. Biomol. Chem., 2026, Advance Article

Synthesis of morpholine derivatives from 1,3-dienes and N-arylaminoalcohols by palladium-catalyzed sequential C–N and C–O bond formation

A. Yamaguchi, N. Katayama, K. Tabaru, T. Fujihara and Y. Obora, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D5OB01744K

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