Results 11 to 20 of about 48,033 (274)

Diastereodivergent nucleophile–nucleophile alkene chlorofluorination

open access: yesNature Chemistry
AbstractThe selective hetero-dihalogenation of alkenes provides useful building blocks for a broad range of chemical applications. Unlike homo-dihalogenation, selective hetero-dihalogenation reactions, especially fluorohalogenation, are underdeveloped. Current approaches combine an electrophilic halogen source with a nucleophilic halogen source, which ...
Sayad Doobary   +6 more
openaire   +4 more sources

Specific nucleophile–electrophile interactions in nucleophilic aromatic substitutions [PDF]

open access: yesOrganic & Biomolecular Chemistry, 2013
We herein report results obtained from an integrated experimental and theoretical study on aromatic nucleophilic substitution (S(N)Ar) reactions of a series of amines towards 1-fluoro-2,4-dinitrobenzene in water. Specific nucleophile-electrophile interactions in the title reactions have been kinetically evaluated.
Ormazábal Toledo, R.   +3 more
openaire   +8 more sources

Multicomponent Molecular Editing of Polybutadiene: From Design Space to Battery Function. [PDF]

open access: yesAdv Sci (Weinh)
Multicomponent molecular editing transforms polybutadiene into an 18‐member polymer library with tunable thermal properties, nanoscale organization, and molecular dynamics. Mapping this multidimensional design space reveals distinct molecular input–property relationships and guides the selection of a candidate electrolyte additive for lithium–sulfur ...
Jeschke J   +8 more
europepmc   +2 more sources

Synthesis of medium-sized rings via nucleophile-induced cascade expansion [PDF]

open access: yes, 2022
This thesis details the development of a novel method for the synthesis of medium-sized lactones and lactams via a cascade process referred to in this thesis as ‘Nucleophile-Induced Cyclisation Expansion’ (NICE).
Glover-Humphreys, William
core   +4 more sources

Control of Nucleophile Chemoselectivity in Cyanobactin YcaO Heterocyclases PatD and TruD [PDF]

open access: yes, 2021
YcaO proteins are ubiquitous in living organisms, where they perform crucial post-translational modifications of peptides and proteins. They are used extensively in biotechnology in companies and academic settings around the world.
Yiwu, Zheng   +4 more
core   +2 more sources

Nucleophile-Controlled Halide Release from the Substitution Reaction of Haloketone for Facet Tuning and Manganese Doping in CsPbCl3 Nanocrystals

open access: yes, 2022
Halide content of the reaction medium not only enhances the brightness of CsPbCl3 nanocrystals but also, control the shape modulations as well as doping Mn­(II) in these host nanocrystals.
Diptam Nasipuri (8662632)   +4 more
core   +1 more source

Handicap-Recover Evolution Leads to a Chemically Versatile, Nucleophile-Permissive Protease. [PDF]

open access: yes, 2015
Mutation of the tobacco etch virus (TEV) protease nucleophile from cysteine to serine causes an approximately ∼104 -fold loss in activity. Ten rounds of directed evolution of the mutant, TEVSer , overcame the detrimental effects of nucleophile exchange ...
Florian Hollfelder   +3 more
core   +3 more sources

Understanding the Nucleophilic Character and Stability of the Carbanions and Alkoxides of 1-(9-Anthryl)ethanol and Derivatives

open access: yesMolecules, 2013
The nucleophilic character and stability of the carbanions vs. alkoxides derived from 2,2,2-trifluoro-1-(9-anthryl)ethanol and 1-(9-anthryl)ethanol containing X electron-releasing and X electron-acceptor substituents attached to C-10, have been studied ...
Francisco Méndez   +2 more
doaj   +1 more source

Nucleophile-Induced Rearrangement of 2H‑Azirine-2-carbonyl Azides to 2‑(1H‑Tetrazol-1-yl)acetic Acid Derivatives

open access: yes, 2021
2H-Azirine-2-carbonyl azides undergo a rearrangement into derivatives of 2-(1H-tetrazol-1-yl)­acetic acid when interacting with O- and S-nucleophiles at room temperature. The reaction is catalyzed by tertiary amines or hydrazoic acid.
Dar’ya V. Spiridonova   +9 more
core   +1 more source

Flavin-N5OOH: A powerful nucleophile and base in nature [PDF]

open access: yes, 2023
Flavoenzymes can mediate a large variety of oxidation reactions via the activation of oxygen. As such, the chemistry of flavoenzymes is an important field that has not yet attained its full scope/recognition. Normally, the O2 activation occurs at the C4a
Qiaoyu, Zhang   +3 more
core   +2 more sources

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