Brønsted acid-catalyzed two-component tandem condensation and cycloisomerization to 6(2 <i>H</i> )-isoquinolinones
An attractive Brønsted acid-catalyzed two-component reaction of 2-alkynyl-4-hydroxybenzaldehydes 1 and primary amines 2 to various 6(2<i>H</i>)-isoquinolinones 3 has been developed. This catalytic system realized an efficient tandem condensation and cycloisomerization reaction to 6(2<i>H</i>)-isoquinolinones 3 in good to excellent yields <i>via</i> a one-pot synthesis, in which two different kinds of C-N bonds were constructed in a straightforward manner. Remarkably, the reaction tolerated various aliphatic, aryl-substituted amines, including chiral amino alcohols and amino acids. The practicality of this approach rendered it a viable alternative for the construction of various 6(2<i>H</i>)-isoquinolinones.
Authors
- Zi‐Sheng Chen (ORCID: https://orcid.org/0000-0001-8778-8889)
- Ke‐Gong Ji (ORCID: https://orcid.org/0000-0001-5707-894X)
- Fang Yang (ORCID: https://orcid.org/0000-0001-6338-8100)
- Yuhua Liu (ORCID: https://orcid.org/0000-0002-7266-1372)
- Linlin Wang (ORCID: https://orcid.org/0000-0001-8634-5357)
- Kexin Wu
Institutions
- Northwest A&F University (CN)
Publication Details
- Journal
- RSC Advances
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5ra01267h
- Primary Topic
- Microbial Natural Products and Biosynthesis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation
- National Natural Science Foundation of China
- Natural Science Foundation of Shaanxi Province