31297-27-5Relevant academic research and scientific papers
Carbene-Catalyzed Reductive Coupling of Nitrobenzyl Bromide and Nitroalkene via the Single-Electron-Transfer (SET) Process and Formal 1,4-Addition
Wang, Yuhuang,Du, Yu,Huang, Xuan,Wu, Xingxing,Zhang, Yuexia,Yang, Song,Chi, Yonggui Robin
supporting information, p. 632 - 635 (2017/02/10)
A carbene-catalyzed reductive 1,4-addition of nitrobenzyl bromides to nitroalkenes is disclosed. The reaction proceeds via a carbene-enabled single-electron-transfer process that generates radicals as key intermediates. The present study expands the potentials of carbene catalysis and offers unusual transformations for common substrates in organic synthesis.
Bimodal ligands with macrocyclic and acyclic binding moieties, complexes and compositions thereof, and methods of using
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, (2010/12/31)
Substituted 1,4,7-triazacyclononane-N,N′,N″-triacetic acid and 1,4,7,10-tetraazacyclcododecane-N,N′,N″,N′″-tetraacetic acid compounds with a pendant amino or hydroxyl group, metal complexes thereof, compositions thereof, and methods of making and use in diagnostic imaging and treatment of cellular disorders.
