Results 151 to 160 of about 255,274 (347)
Oxygen Vacancies in β-MoO<sub>3</sub> Mediate Imine Synthesis via Reductive Coupling of Nitro Compounds and Alcohols. [PDF]
Yuan Z +5 more
europepmc +1 more source
Chemical Methods for Peptide and Protein Backbone Cleavage
Protein cleavage plays essential roles in biology and is powerful for protein manipulation and functionalization as well as in recombinant expression and purification. Here, the historical background and most recent examples of chemical methods for protein and peptide backbone cleavage are discussed (part of the figure was generated in BioRender).
Miguel Angel Alena‐Rodriguez +1 more
wiley +1 more source
A Computational Study of the NMR Chemical Shifts of Polynitropyrazoles. [PDF]
Alcorta A +3 more
europepmc +1 more source
The cis‐2,3‐bis(trifluoromethyl)cyclopropyl chemotype is introduced. The steric demand of this motif is intermediate between that of the heptafluoroisopropyl and prefluorotertbutyl groups; yet, it induces significantly less lipophilicity than these due to its facial polarity.
Daniel Gaviña +5 more
wiley +1 more source
Plasma-activated solutions reverse chronic deltamethrin exposure induced intestinal injury via rebalancing redox homeostasis and counteracting cellular senescence. [PDF]
Deng X +18 more
europepmc +1 more source
Cathepsin B‐sensitive peptide–adjuvant conjugates are designed, synthesized, and evaluated to deliver an antigenic peptid and an adjuvant targeting Toll‐like receptors 7 and 8 (TLR7/8) to antigen presenting cells. The adjuvant is released by cathepsin B resulting in antigen presentation and TLR mediated T cell activation.
Marjolein M. E. Isendoorn +6 more
wiley +1 more source
Fluorescent solvatochromism and nonfluorescence processes of charge-transfer-type molecules with a 4-nitrophenyl moiety. [PDF]
Miwa M, Ito A.
europepmc +1 more source
LXXXIX.—The ortho- and para-nitro-derivatives of orthotoluidine
Arthur G. Green, Thos. A. Lawson
openalex +1 more source
Skeletal Editing from Pyridine to Aniline via C‐Insertion and N‐Isomerization
A concise protocol is presented that converts pyridines into anilines by externalizing the original pyridine nitrogen at either the "ipso" or "ortho" position, which results in para or meta‐primary aniline products. A key carbene‐insertion step precedes nitrogen migration, preserving both ring size and overall structure.
Yun Luo +3 more
wiley +1 more source

