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.

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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
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article

Pathway economy in cyclization of 1 ,n -enynes

Lu Yang, Hyunsoo Han, Bin Lin, Maosheng Cheng et al.
Beilstein Journal of Organic Chemistry
Catalytic Alkyne Reactions
article

Pathway economy in cyclization of 1 ,n -enynes

Lu Yang, Hyunsoo Han, Bin Lin, Maosheng Cheng, Yongxiang Liu, W. Mao
article en

Abstract

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.

Beilstein Journal of Organic ChemistryVol. 21
Shenyang Pharmaceutical University (CN)
Openalex Percentile: Top 77%
Catalytic Alkyne Reactions
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