Tungsten-Mediated Coupling of Dienes and Anilines for the Construction of 1,4-Amino Alcohols

Abstract A practical, efficient, and scalable procedure has been established for the general synthesis of 1,4-amino alcohols from anilines and dienes in a single operation. This method constitutes a valuable alternative to most existing processes based on nitrosobenzene. The ready availability of starting materials and the use of a readily accessible W(VI) precatalyst collectively render this approach attractive for library construction of 1,4-amino alcohol compounds. The results highlight a beneficial steric effect at the tungsten center, with bulkier groups correlating with improved catalytic performance.

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Publication Details

Journal
Organic Letters
Published
2026-10-28
DOI
https://doi.org/10.1021/acs.orglett.6c04442
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Tungsten-Mediated Coupling of Dienes and Anilines for the Construction of 1,4-Amino Alcohols

Fu Yang, Heng Song, Chen Xu, Shaojun Zheng et al.
1 links
Organic Letters
Catalytic Alkyne Reactions
article

Tungsten-Mediated Coupling of Dienes and Anilines for the Construction of 1,4-Amino Alcohols

Fu Yang, Heng Song, Chen Xu, Shaojun Zheng, Yougen Cai, Ying Li, Jiahao Wang, Xingwei Cai
article en

Abstract

Abstract A practical, efficient, and scalable procedure has been established for the general synthesis of 1,4-amino alcohols from anilines and dienes in a single operation. This method constitutes a valuable alternative to most existing processes based on nitrosobenzene. The ready availability of starting materials and the use of a readily accessible W(VI) precatalyst collectively render this approach attractive for library construction of 1,4-amino alcohol compounds. The results highlight a beneficial steric effect at the tungsten center, with bulkier groups correlating with improved catalytic performance.

Organic Letters
Jiangsu University of Science and Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 26%
Catalytic Alkyne Reactions
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