Hexafluoroisopropanol-Mediated Hydroaminoalkylation–Aza-Prins for Construction of α-Amino-butenolide

The widespread presence of butenolide motifs in pharmaceuticals, natural products, and small-molecule biological probes has continuously motivated the development of efficient synthetic strategies. Herein, we describe a practical and broadly applicable strategy for the construction of highly functionalized butenolides through an HFIP-mediated three-component cascade hydroaminoalkylation-aza-Prins reaction under metal-free conditions. The structural and functional diversity of the readily accessible secondary amines, keto acids, and allenes offers a versatile and flexible platform for the rapid construction of valuable butenolides. The versatility of the developed protocol is underscored by its successful application to the late-stage functionalization of medicinally relevant complex molecules and natural products.

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Journal
Organic Letters
Published
2026-03-09
DOI
https://doi.org/10.1021/acs.orglett.6c00340
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
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article

Hexafluoroisopropanol-Mediated Hydroaminoalkylation–Aza-Prins for Construction of α-Amino-butenolide

Zhongyi Zeng, Shengdong Wang, Wei Yi, Jianlian Huang et al.
Organic Letters
Synthetic Organic Chemistry Methods
article

Hexafluoroisopropanol-Mediated Hydroaminoalkylation–Aza-Prins for Construction of α-Amino-butenolide

Zhongyi Zeng, Shengdong Wang, Wei Yi, Jianlian Huang, Zhi Zhou
article en

Abstract

The widespread presence of butenolide motifs in pharmaceuticals, natural products, and small-molecule biological probes has continuously motivated the development of efficient synthetic strategies. Herein, we describe a practical and broadly applicable strategy for the construction of highly functionalized butenolides through an HFIP-mediated three-component cascade hydroaminoalkylation-aza-Prins reaction under metal-free conditions. The structural and functional diversity of the readily accessible secondary amines, keto acids, and allenes offers a versatile and flexible platform for the rapid construction of valuable butenolides. The versatility of the developed protocol is underscored by its successful application to the late-stage functionalization of medicinally relevant complex molecules and natural products.

Organic LettersVol. 28(11)
Target (United States) (US), State Key Laboratory of Respiratory Disease (CN), Guangzhou Medical University (CN)
Openalex Percentile: Top 28%
Synthetic Organic Chemistry Methods
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