计算机科学
自然(考古学)
丁烯内酯
协议(科学)
纳米技术
功能多样性
工程类
生化工程
级联
合成生物学
化学
作者
Jianlian Huang,Zhongyi Zeng,Zhi Zhou,Wei Yi,Shengdong Wang
出处
期刊:PubMed
[National Institutes of Health]
日期:2026-03-09
标识
DOI:10.1021/acs.orglett.6c00340
摘要
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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