Pathway economy in cyclization of 1 <i>,n</i> -enynes
This review presents a paradigm-shifting "pathway economy" strategy for 1,<i>n</i>-enyne cyclization, enabling divergent construction of complex molecular architectures from a single substrate class. Through mechanistic-guided modulation of catalysts, solvents, ligands, and angle strain, this approach achieves unprecedented reaction pathway control while demonstrating superior temporal and step efficiency compared to conventional methods. The work establishes a sustainable framework for rapid molecular diversification, offering transformative potential for green chemistry and pharmaceutical applications. By unifying mechanistic insights with practical synthetic design, this review provides valuable guidance for future innovations in precision organic synthesis.
Authors
- Lu Yang (ORCID: https://orcid.org/0000-0001-9727-4849)
- Hyunsoo Han (ORCID: https://orcid.org/0000-0001-7821-5851)
- Bin Lin (ORCID: https://orcid.org/0000-0003-2369-4765)
- Maosheng Cheng (ORCID: https://orcid.org/0000-0001-9073-4806)
- Yongxiang Liu (ORCID: https://orcid.org/0000-0003-0364-0137)
- W. Mao (ORCID: https://orcid.org/0009-0006-6862-8146)
Institutions
- Shenyang Pharmaceutical University (CN)
Publication Details
- Journal
- Beilstein Journal of Organic Chemistry
- Published
- 2025-10-27
- DOI
- https://doi.org/10.3762/bjoc.21.173
- Primary Topic
- Catalytic Alkyne Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00