Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Nikita, Chekshin"'
Autor:
Guangrong Meng, Zhen Wang, Hau Sun Sam Chan, Nikita Chekshin, Zhen Li, Peng Wang, Jin-Quan Yu
Publikováno v:
Journal of the American Chemical Society. 145:8198-8208
Publikováno v:
ACS Catalysis. 12:10581-10586
Publikováno v:
Journal of the American Chemical Society. 144:4727-4733
Publikováno v:
J Am Chem Soc
Pd(II)-catalyzed site-selective β- and γ-C(sp(3))−H arylation of primary aldehydes is developed by rational design of L,X-type transient directing groups (TDG). External 2-pyridone ligands are identified to be crucial for the observed reactivity.
Autor:
Shaoqun Qian, Nikita Chekshin, Zhe Zhuang, Jennifer X. Qiao, Zhen Wang, Liang Hu, Jin-Quan Yu
Publikováno v:
Science. 374:1281-1285
Dehydrogenative transformations of alkyl chains to alkenes through methylene carbon-hydrogen (C–H) activation remain a substantial challenge. We report two classes of pyridine-pyridone ligands that enable divergent dehydrogenation reactions through
Autor:
Kap-Sun Yeung, William R. Ewing, Jin-Quan Yu, Zhen Li, Shaoqun Qian, Nikita Chekshin, Zhen Wang, Jennifer X. Qiao, Peter T. W. Cheng
Publikováno v:
Science
Easing oxygen into arenes Although oxygen is all around us, it is often surprisingly difficult to use it for selective chemical oxidations, necessitating more expensive, wasteful alternatives. Li et al. report that careful ligand optimization produce
Publikováno v:
Journal of the American Chemical Society. 142:5117-5125
Saturated azacycles are commonly encountered in bioactive compounds and approved therapeutic agents. The development of methods for functionalization of the α-methylene C-H bonds of these highly privileged building blocks is of great importance, esp
Pd(II)-catalyzed site-selective β- and γ-C(sp3)−H arylation of primary aldehydes is developed by rational design of L,X-type transient directing groups (TDG). External 2-pyridone ligands are identified to be crucial for the observed reactivity. B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a4f878a3ed24f3cdfb2fda7616f9b22
https://doi.org/10.26434/chemrxiv-2022-bt3z4
https://doi.org/10.26434/chemrxiv-2022-bt3z4
Autor:
Daniel C. Schmitt, Paul F. Richardson, Tyler G. Saint-Denis, Jason S. Chen, Yajing Lian, Kevin D. Hesp, Nelson Y. S. Lam, Nikita Chekshin, Jin-Quan Yu, Chan Woo Huh, Jeff Elleraas
Publikováno v:
ACS Catal
Enantioselective C(sp(3))–H activation has gained considerable attention from the synthetic chemistry community. Despite the intense interest in these reactions, the mechanisms responsible for enantioselection are still vague. In the course of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3289d8d5c73f1ac6d9aa498e6a1e083a
https://europepmc.org/articles/PMC9098185/
https://europepmc.org/articles/PMC9098185/
Autor:
Pritha Verma, Erika L. Lucas, Jin-Quan Yu, Tyler G. Saint-Denis, Nikita Chekshin, Nelson Y. S. Lam, Guangrong Meng
Publikováno v:
J Am Chem Soc
The ability to differentiate between highly similar C-H bonds in a given molecule remains a fundamental challenge in organic chemistry. In particular, the lack of sufficient steric and electronic differences between C-H bonds located distal to functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b8d882558dde1617e97d3892740e6bd
https://europepmc.org/articles/PMC7485751/
https://europepmc.org/articles/PMC7485751/