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1.
J Org Chem ; 88(24): 17538-17543, 2023 Dec 15.
Article in English | MEDLINE | ID: mdl-38033293

ABSTRACT

We have established hydrogen atom transfer (HAT) as the key player in a directed, photopromoted fluorination of pyridylic groups. The Lewis basic pyridyl nitrogen directs amine radical dication propagated HAT and Selectfluor fluorination of various ortho substituents in a highly regioselective manner with little to no side product formation. A variety of pyridines and quinolines were employed to showcase the directing capability of the nitrogen atom. Additionally, both experimental and computational data are provided that illuminate how this mechanism differs from and complements prior work in the area.

2.
J Org Chem ; 88(11): 7597-7600, 2023 Jun 02.
Article in English | MEDLINE | ID: mdl-37159569

ABSTRACT

In this note, we explore a unique reactivity pattern that involves a rare radical-based C-C bond scission of epoxides followed by demethylenation. The reaction is accomplished by Selecfluor and its radical dication working in tandem; a mechanism supported by experiment and DFT calculations is proposed that involves the generation and identification of a key reactive intermediate. The reaction seems to be fairly general for 1,1-disubstituted epoxides.

3.
Int J Mol Sci ; 21(11)2020 Jun 04.
Article in English | MEDLINE | ID: mdl-32512831

ABSTRACT

Renal fibrosis is a common fate of chronic kidney diseases. Emerging studies suggest that unsolved inflammation will progressively transit into tissue fibrosis that finally results in an irreversible end-stage renal disease (ESRD). Renal inflammation recruits and activates immunocytes, which largely promotes tissue scarring of the diseased kidney. Importantly, studies have suggested a crucial role of innate immunity in the pathologic basis of kidney diseases. This review provides an update of both clinical and experimental information, focused on how innate immune signaling contributes to renal fibrogenesis. A better understanding of the underlying mechanisms may uncover a novel therapeutic strategy for ESRD.


Subject(s)
Disease Susceptibility/immunology , Immunity, Innate , Renal Insufficiency, Chronic/etiology , Renal Insufficiency, Chronic/metabolism , Animals , Biomarkers , Fibrosis , Humans , Immunosuppression Therapy , Macrophages/immunology , Macrophages/metabolism , Macrophages/pathology , Myofibroblasts/immunology , Myofibroblasts/metabolism , Renal Insufficiency, Chronic/pathology , Signal Transduction
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