42245-33-0Relevant academic research and scientific papers
Dual PPAR-delta and PPAR-gamma agonists
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Sheet 24, (2020/12/07)
The present invention relates to compositions and methods using for activating Peroxisomal Proliferator Activating Receptor (PPAR)-β/δ and/or PPAR-γ. In some embodiments, the present invention relates to compounds and methods of treating a disease or disorder associated with PPAR-β/δ and/or PPAR-γ. In some embodiments, present invention relates to compounds and methods of treating Alzheimer's disease, diabetes, and reduced cognition.
Fe(III)-Catalyzed Aerobic Intramolecular N-N Coupling of Aliphatic Azides with Amines
Zhang, Yue,Duan, Dongyu,Zhong, Ying,Guo, Xin-Ai,Guo, Jiawei,Gou, Jing,Gao, Ziwei,Yu, Binxun
supporting information, p. 4960 - 4965 (2019/09/03)
An Fe(III)-catalyzed intramolecular N-N coupling of aliphatic azidoamines that forms diverse five- and six-membered semisaturated diazoheterocycles using air as an oxidant is reported, providing an alternative to hydrazine-based methods. Mechanistic studies suggest that a N-radical induced intramolecular homolytic substitution (SH2) is involved in ring closure. The power of this N-N bond-forming method is also demonstrated by using it as the final step in a total synthesis of (-)-newbouldine.
A twin-axial hetero[7]rotaxane
Zhang, Zhi-Jun,Zhang, Heng-Yi,Wang, Hui,Liu, Yu
supporting information; experimental part, p. 10834 - 10838 (2011/12/16)
Two in one: Two pseudorotaxanes can be combined to form a twin-axial hetero[7]rotaxane (see picture) by using the copper-catalyzed alkyne-azide "click" reaction. The synthetic route, in which twin-axial and single-axial rotaxanes are formed, combines self
Synthesis of substituted piperidines, indolizidines, quinolizidines, and pyrrolizidines via a cycloaddition strategy using acetylenic sulfones as alkene dipole equivalents
Back, Thomas G.,Nakajima, Katsumasa
, p. 261 - 263 (2008/02/13)
(equation presented) The conjugate additions of β- and γ-chloroamines to acetylenic sulfones afford enamine sulfones, which then undergo intramolecular alkylation to produce the corresponding cyclic enamines. This provides a convenient route to substitute
