Results 21 to 30 of about 253,250 (328)

Thiol-linked alkylation of RNA to assess expression dynamics

open access: yesNature Methods, 2017
Gene expression profiling by high-throughput sequencing reveals qualitative and quantitative changes in RNA species at steady state but obscures the intracellular dynamics of RNA transcription, processing and decay.
Veronika A. Herzog   +9 more
semanticscholar   +1 more source

Poly(thioether) vitrimers via transalkylation of trialkylsulfonium salts [PDF]

open access: yes, 2017
Vitrimers are permanently cross-linked organic polymers that can be reshaped, molded, and recycled without loss of network integrity. Herein, we report poly(thioether) networks, prepared through a straightforward thiol-ene photopolymerization, that can ...
Hendriks, Benjamin   +3 more
core   +1 more source

Lead-Halide Perovskites for Photocatalytic α-Alkylation of Aldehydes.

open access: yesJournal of the American Chemical Society, 2019
Cost-effective and efficient photocatalysis are highly desirable in chemical synthesis. Here we demonstrate that readily prepared suspensions of APbBr3 (A = Cs or methylammonium (MA)) type perovskite colloids (ca.
Xiaolin Zhu   +4 more
semanticscholar   +1 more source

3-(2-Diisopropylaminoethyl)-5-(4-methoxybenzylidene)thiazolidine-2,4-dione

open access: yesMolbank, 2022
Thiazolidine-2,4-dione core is widely used in the medicinal chemistry of different types of potential drug-like small molecules. In the present work, the synthesis of a novel non-condensed thiazolidine-2,4-dione-bearing derivative is reported by the two ...
Serhii Holota   +3 more
doaj   +1 more source

On the prevalence of bridged macrocyclic pyrroloindolines formed in regiodivergent alkylations of tryptophan. [PDF]

open access: yes, 2016
A Friedel-Crafts alkylation is described that efficiently transforms tryptophan-containing peptides into macrocycles of varying ring connectivity. Factors are surveyed that influence the distribution of regioisomers, with a focus on indole C3-alkylations
Curtin, Brice H   +5 more
core   +1 more source

Open-Air Alkylation Reactions in Photoredox-Catalyzed DNA-Encoded Library Synthesis.

open access: yesJournal of the American Chemical Society, 2019
DNA-encoded library (DEL) technology is a powerful tool commonly used by the pharmaceutical industry for the identification of compounds with affinity to biomolecular targets. Success in this endeavor lies in sampling diverse chemical libraries. However,
J. Phelan   +7 more
semanticscholar   +1 more source

Regioselective Alkylation of an Oxonaphthalene-Annelated Pyrrol System

open access: yesMolbank, 2009
The regioselective alkylation of an oxonaphthalene-annelated pyrrole system is reported. The regioselectivity of alkylation can be controlled by the selection of the solvent.
Helmut Spreitzer, Christiane Puschmann
doaj   +1 more source

Progress of decreasing toxic polycyclic aromatic hydrocarbons content in coal-tar pitch by alkylation method

open access: yesMeitan kexue jishu, 2023
Coal-tar pitch (CTP) is a substance produced by ambient and/or vacuum distillation of high-temperature coal tar, although CTP has a large yield in China, however its wide application is limited due to its high toxicity.
ZHANG Wenshuo   +5 more
doaj   +1 more source

Visible Light-Enabled Direct Decarboxylative N-Alkylation.

open access: yesAngewandte Chemie, 2020
Development of efficient and selective C-N bond-forming reactions from abundant feedstock chemicals remains a central theme in organic chemistry, due to the key roles of amines in synthesis, drug discovery and materials science.
V. Nguyen   +6 more
semanticscholar   +1 more source

Unanticipated differences between α- and γ-diaminobutyric acid-linked hairpin polyamide-alkylator conjugates [PDF]

open access: yes, 2006
Hairpin polyamide–chlorambucil conjugates containing an {alpha}-diaminobutyric acid ({alpha}-DABA) turn moiety are compared to their constitutional isomers containing the well-characterized {gamma}-DABA turn.
Chou, C. James   +4 more
core   +4 more sources

Home - About - Disclaimer - Privacy