Deciphering complexity in Pd-catalyzed cross-couplings

被引:6
作者
Clarke, George E. [1 ]
Firth, James D. [1 ]
Ledingham, Lyndsay A. [1 ]
Horbaczewskyj, Chris S. [1 ]
Bourne, Richard A. [2 ,3 ]
Bray, Joshua T. W. [1 ]
Martin, Poppy L. [1 ]
Eastwood, Jonathan B. [1 ]
Campbell, Rebecca [1 ]
Pagett, Alex [1 ]
Macquarrie, Duncan J. [1 ]
Slattery, John M. [1 ]
Lynam, Jason M. [1 ]
Whitwood, Adrian C. [1 ]
Milani, Jessica [1 ]
Hart, Sam [1 ]
Wilson, Julie [4 ]
Fairlamb, Ian J. S. [1 ]
机构
[1] Univ York, Dept Chem, York YO10 5DD, England
[2] Univ Leeds, Inst Proc Res & Dev, Sch Chem, Leeds LS2 9JT, England
[3] Univ Leeds, Sch Chem & Proc Engn, Leeds LS2 9JT, England
[4] Univ York, Dept Math, York YO10 5DD, England
基金
英国工程与自然科学研究理事会;
关键词
HIGH-THROUGHPUT EXPERIMENTATION; FORMING REDUCTIVE ELIMINATION; ARYL HALIDES; SUZUKI-MIYAURA; PALLADIUM; HECK; MECHANISM; LIGAND; ARYLATION; ACID;
D O I
10.1038/s41467-024-47939-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding complex reaction systems is critical in chemistry. While synthetic methods for selective formation of products are sought after, oftentimes it is the full reaction signature, i.e., complete profile of products/side-products, that informs mechanistic rationale and accelerates discovery chemistry. Here, we report a methodology using high-throughput experimentation and multivariate data analysis to examine the full signature of one of the most complicated chemical reactions catalyzed by palladium known in the chemical literature. A model Pd-catalyzed reaction was selected involving functionalization of 2-bromo-N-phenylbenzamide and multiple bond activation pathways. Principal component analysis, correspondence analysis and heatmaps with hierarchical clustering reveal the factors contributing to the variance in product distributions and show associations between solvents and reaction products. Using robust data from experiments performed with eight solvents, for four different reaction times at five different temperatures, we correlate side-products to a major dominant N-phenyl phenanthridinone product, and many other side products. Knowledge about the full reaction signature, such as the complete profile of products and side-products is important in accelerating discovery chemistry. Here, the authors report a methodology using high-throughput experimentation and multivariate data analysis to examine Palladium- catalyzed cross-coulpling reactions.
引用
收藏
页数:15
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