Results 41 to 50 of about 1,216 (196)

Diverse reactivity of maleimides in polymer science and beyond

open access: yesPolymer International, Volume 74, Issue 4, Page 296-306, April 2025.
This mini‐review provides a thorough overview of maleimide chemistry, highlighting its diverse reactivity in polymer and materials science applications. Abstract Maleimides are remarkably versatile functional groups, capable of participating in homo‐ and copolymerizations, Diels–Alder and (photo)cycloadditions, Michael additions, and other reactions ...
Bruce E Kirkpatrick   +2 more
wiley   +1 more source

Synthesis of New 2-Halo-2-(1H-tetrazol-5-yl)-2H-azirines via a Non-Classical Wittig Reaction

open access: yesMolecules, 2015
The synthesis and reactivity of tetrazol-5-yl-phosphorus ylides towards N-halosuccinimide/TMSN3 reagent systems was explored, opening the way to new haloazidoalkenes bearing a tetrazol-5-yl substituent.
Ana L. Cardoso   +4 more
doaj   +1 more source

Singlet Photoreactivity of 3-Methyl-2-phenyl-2H-azirine

open access: yes, 2017
Irradiation of 3-methyl-2-phenyl-2H-azirine (1) at 254 nm in argon matrices results in ylide 6. Similarly, laser flash photolysis (λ = 266 nm) of azirine 1 in acetonitrile yields ylide 6, which has a transient absorption with λmax at ~340 nm and a ...
Bruce S. Ault   +6 more
core   +1 more source

Light-induced synthesis of 2H-azirines and its applications in organic chemistry

open access: yesJournal of Saudi Chemical Society
2H-azirines have represented versatile building motifs in the domain of organic chemistry owing to their excellent reaction activity induced by the high strain of the three-membered ring species.
Shibo Lin   +4 more
doaj   +1 more source

Oxaziridines: Versatile Reagents in Modern Organic Synthesis

open access: yesThe Chemical Record, EarlyView.
Being capable of transferring an O atom and N‐group/atom, oxaziridines are considered multitasking agents. These are employed for diverse organic transformations, such as epoxidation of olefins, α‐ and γ‐hydroxylation/amination of carbonyl compounds, oxidation of sulfides, [3+2]cycloaddition with unsaturated systems.
Ajeet Chandra   +2 more
wiley   +1 more source

Enantioselective addition of organolithium reagents to a 2H-azirine

open access: yes, 2002
3-(2-Naphthyl)-2H-azirine was used as a model substrate in the first enantioselective addition of organolithium reagents to an azirine. Various organolithium reagents have been used together with different chiral ligands.
Somfai, Peter,, Risberg, E.
core   +1 more source

2‑Diazoacetyl‑2H‑azirines: Source of a Variety of 2H‑Azirine Building Blocks with Orthogonal and Domino Reactivity

open access: yes, 2018
A synthesis of 2-diazoacetyl-2H-azirines was developed starting from 2H-azirine-2-carbonyl chlorides, generated by Fe­(II)-catalyzed isomerization of 5-chloroisoxazoles. 2-Diazoacetyl-2H-azirines easily undergo reactions characteristic of α-diazo ketones
Pavel A. Sakharov (5519120)   +2 more
core   +2 more sources

Chemical Metabolomics: Chemical Biology Tools for Advanced Metabolism Investigations

open access: yesAngewandte Chemie, Volume 138, Issue 23, 1 June 2026.
The human metabolism has been investigated for several millennia. The metabolome is known for a high complexity due to a large number of different metabolites that are present at different concentrations. Metabolomics has been developed as a field to investigate the entire human metabolome and to elucidate disease development mechanisms.
Alejandro Torregrosa‐Chinillach   +4 more
wiley   +2 more sources

Ethyl 3-(2-pyridyl)-2H-azirine-2-carboxylate : synthesis and reactivity with dienes [PDF]

open access: yes, 2012
Ethyl 3-(2-pyridyl)-2H-azirine-2-carboxylate, the first example of an 3-heteroamatic 2H-azirine has been prepared. The reaction of ethyl 3-(2-pyridyl)-2H-azirine-2-carboxylate with conjugated 1,3-dienes, under mild conditions and in the absence of ...
Alves, Maria José Chão   +3 more
core   +1 more source

Ethyl 3-(2-pyridyl)-2H-azirine-2-carboxylate : synthesis and reactivity with dienes [PDF]

open access: yes, 2005
Ethyl 3-(2-pyridyl)-2H-azirine-2-carboxylate, the first example of an 3-heteroamatic-2H-azirine, was prepared and its reaction with conjugated 1,3-dienes, under mild conditions and in the absence of Lewis acid catalyst, produced cycloadducts in good ...
Alves, M. José   +3 more
core   +1 more source

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