574-45-8Relevant articles and documents
An unexpected base-induced rearrangement of tritylamine
Theodorou, Vassiliki,Skobridis, Konstantinos
, p. 5021 - 5023 (2005)
An unexpected rearrangement was observed during the treatment of tritylamine with n-butyllithium, leading to the formation of an imine.
Novel functional groups with fine-controlled metal assembling function
Yamamoto, Kimihisa,Higuchi, Masayoshi,Kimoto, Atsushi,Imaoka, Takane,Masachika, Kiriko
, p. 349 - 355 (2005)
Half-substituted dendritic phenylazomethine dendrimers with various substituents (Half-DPA-X Gn, where n is the generation number) were synthesized in order to elucidate the electron gradients in the dendrons by complexation with metal ions. Along with th
New condensation of potassium diphenylketyl and its dianion with aniline
Turaeva,Kurbatov
, p. 1691 - 1692 (2002)
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Iodine-mediated 1,2-aryl migration of primary benzhydryl amines
Chang, Junbiao,Du, Yangxu,Hao, Wei,Hou, Jiao,Lu, Qing,Yu, Wenquan
supporting information, p. 16223 - 16226 (2021/09/22)
An iodine-mediated 1,2-aryl migration reaction of primary benzhydryl amines under transition metal-free conditions has been achieved. The crude imines generated by this rearrangement reaction can be directly transformed into various aromatic secondary ami
Copper-Catalysed Electrophilic Amination of Aryl(alkenyl) Boronic Acids with Nitrogen-Containing Hypervalent Iodine (III) Reagent
Hu, Yuanyuan,Zheng, Songlin,Fan, Wu,Yuan, Weiming
supporting information, p. 4701 - 4707 (2021/08/23)
A copper-catalysed electrophilic N-imination of aryl(alkenyl) boronic acids with a stable hypervalent iodine(III) reagent containing a transferable (diarylmethylene)amino group is developed. The electrophilic C?N cross-coupling reaction proceeds smoothly at room temperature under oxidant-free and base-free conditions, which is further characterized by the broad functional group compatibility, thereof, extending the N-electrophile scope of electrophilic C?N cross-coupling outside the limitation of N?O and N?Cl reagents. (Figure presented.).