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.
Authors
- Zhongyi Zeng (ORCID: https://orcid.org/0000-0003-3366-7592)
- Shengdong Wang (ORCID: https://orcid.org/0000-0001-7431-2515)
- Wei Yi (ORCID: https://orcid.org/0000-0002-8432-4007)
- Jianlian Huang
- Zhi Zhou
Institutions
- Target (United States) (US)
- State Key Laboratory of Respiratory Disease (CN)
- Guangzhou Medical University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-03-09
- DOI
- https://doi.org/10.1021/acs.orglett.6c00340
- Primary Topic
- Synthetic Organic Chemistry Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00