Journal of Controlled Release, Journal Year: 2025, Volume and Issue: 384, P. 113887 - 113887
Published: May 26, 2025
Language: Английский
Journal of Controlled Release, Journal Year: 2025, Volume and Issue: 384, P. 113887 - 113887
Published: May 26, 2025
Language: Английский
The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: 90(4), P. 1683 - 1696
Published: Jan. 17, 2025
In the vanguard of sustainable chemistry, pursuit efficient pathways for synthesis alkyl bicyclo[1.1.1]pentane-heteroaryls has captured attention scientific vanguard. We herein report a groundbreaking and eco-conscious multicomponent coupling reaction that paves way alkylation heteroarylation [1.1.1]propellane, process uniquely enabled by photochemical prowess an electron donor–acceptor (EDA) complex. This method is distinguished its minimalist yet powerful approach: devoid transition metals, additives, photosensitizers. Its universality further exemplified seamless compatibility broad spectrum halides heteroarenes under standardized conditions, heralding new era synthetic versatility. The method's practicality underscored capacity late-stage modification pharmaceuticals, offering transformative tool enhancement existing drug molecules. Moreover, facile derivatization synthesized products underscores adaptability potential diverse applications. Our mechanistic studies have elucidated underlying radical-relay pathway, pinpointing pivotal role EDA complex in initiating transformation. discovery not only enriches our fundamental understanding but also opens avenues strategic optimization.
Language: Английский
Citations
6Organic Letters, Journal Year: 2025, Volume and Issue: 27(10), P. 2526 - 2531
Published: March 5, 2025
Herein, we introduce an efficient and straightforward strategy for the selective C-H esterification alkylation of quinoxalin-2(1H)-ones with aldehydes. A key feature our study is ability to perform both using different types The reaction system highly compatible a range aldehydes, yielding C3-esterified C3-alkylated products in moderate-to-good yields. applicability this approach further enhanced by its scalability through continuous-flow synthesis, late-stage modification significant molecules, product derivatization. Our mechanistic investigations reveal radical relay mechanism, triggered hydrogen atom transfer process.
Language: Английский
Citations
5Organic Letters, Journal Year: 2025, Volume and Issue: unknown
Published: April 26, 2025
Herein, a photoinduced heterogeneous catalytic system merging g-C3N4 and NaI has been established for the difunctionalization of alkenes in conjunction with heteroarenes methyl carbazate. This approach is notable its broad substrate tolerance, encompassing wide range leading to formation corresponding esters moderate good yields. Additionally, scalability synthetic process versatility product transformations have illustrated, highlighting potential practical application organic synthesis.
Language: Английский
Citations
2Journal of Controlled Release, Journal Year: 2025, Volume and Issue: 384, P. 113887 - 113887
Published: May 26, 2025
Language: Английский
Citations
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