Application In Synthesis of 1-(tert-Butyl)-1H-pyrrole-2,5-dione. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 1-(tert-Butyl)-1H-pyrrole-2,5-dione, is researched, Molecular C8H11NO2, CAS is 4144-22-3, about Rhodium-Catalyzed Vinylic C-H Functionalization of Enol Carbamates with Maleimides. Author is Sharma, Satyasheel; Han, Sang Hoon; Jo, Hyeim; Han, Sangil; Mishra, Neeraj Kumar; Choi, Miji; Jeong, Taejoo; Park, Jihye; Kim, In Su.
The rhodium(III)-catalyzed direct C-H functionalization of enol carbamates with a range of maleimides is described. With the assistance of the carbamoyl directing group, this reaction provides biol. relevant succinimide compounds by proceeding through a C-Rh addition and subsequent protonation pathway.
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Chloride – Wikipedia,
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