Results 11 to 20 of about 3,434 (226)

Synthesis of trifluoromethylated 2H-azirines through Togni reagent-mediated trifluoromethylation followed by PhIO-mediated azirination [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2018
The reaction of enamine compounds with the Togni reagent in the presence of CuI afforded β-trifluoromethylated enamine intermediates, which were converted directly to biologically interesting trifluoromethylated 2H-azirines by an iodosobenzene (PhIO ...
Jiyun Sun   +5 more
doaj   +3 more sources

Enantiomerically Enriched Aziridine-2-carboxylates via Copper-Catalyzed Reductive Kinetic Resolution of 2H-Azirines [PDF]

open access: yesAngewandte Chemie, Volume 137, Issue 26, June 24, 2025.
We present the first reductive kinetic resolution of racemic 2H-azirines to prepare optically enriched N-H aziridine-2-carboxylates, which are bench stable and easily diversifiable building blocks, concomitantly with the corresponding enantiomerically ...
Chiu, Pauline   +3 more
core   +3 more sources

Diastereoselective ZnCl2-Mediated Joullié–Ugi Three-Component Reaction for the Preparation of Phosphorylated N-Acylaziridines from 2H-Azirines [PDF]

open access: yesMolecules
We disclose a direct approach to the diastereoselective synthesis of phosphorus substituted N-acylaziridines based on a one-pot ZnCl2-catalyzed Joullié–Ugi three-component reaction of phosphorylated 2H-azirines, carboxylic acids and isocyanides.
Julene Allende   +4 more
doaj   +2 more sources

Synthesis and Application of Bioactive N-Functionalized Aziridines. [PDF]

open access: yesAngew Chem Int Ed Engl
This review discusses modern synthetic methods for the preparation of aziridine‐containing small molecules, including biocatalytic, electrocatalytic, and photocatalytic strategies. We highlight the compatibility of various synthetic methods with control of the exocyclic N‐substituent.
Tan H   +4 more
europepmc   +3 more sources

Polymerization-Induced Direct Photolithography of Quantum Dots. [PDF]

open access: yesMacromol Rapid Commun
We present a comprehensive overview of photochemical polymerization strategies for direct lithographic patterning of colloidal quantum dots (QDs). Reaction mechanisms are categorized by functional group type, and their application is discussed in terms of pattern fidelity, photostability, and environmental robustness, highlighting the potential of ...
Kim T, Gwak N, Oh N, Kim TA.
europepmc   +2 more sources

Isomerization of 5-(2H-Azirin-2-yl)oxazoles: An Atom-Economic Approach to 4H-Pyrrolo[2,3-d]oxazoles

open access: yesMolecules, 2021
An atom economical method for the preparation of variously substituted 4H-pyrrolo[2,3-d]oxazoles was developed on the basis of thermal isomerization of 5-(2H-azirin-2-yl)oxazoles.
Timur O. Zanakhov   +4 more
doaj   +1 more source

2H-Azirines as dipolarophiles [PDF]

open access: yesTetrahedron Letters, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Melo, Teresa M. V. D. Pinho e   +3 more
openaire   +2 more sources

CN and CCH azirine derivatives, possible precursors of prebiotic molecules: Formation and spectroscopic parameters

open access: yesMonthly notices of the Royal Astronomical Society, 2023
N-heterocycles are of special relevance in astrobiology but at present no nitrogen-containing heterocycles have been detected in the interstellar medium (ISM).
P. Redondo, M. Sanz-Novo, C. Barrientos
semanticscholar   +1 more source

Structure, spectroscopic signatures and formation of hydroxy-azirine: a potential interstellar prebiotic molecule

open access: yesMonthly notices of the Royal Astronomical Society, 2023
Hydroxy-azirine (C2H3NO) is a -OH derivative of azirine (C2H3N), molecule that has been the subject of several unfruitful searches in space. Hydroxy-azirine is an isomer of the detected prebiotic species methyl isocyanate, CH3NCO, and glycolonitrile ...
P. Redondo   +3 more
semanticscholar   +1 more source

Synthesis of Siphonazole B Through Domino Cycloisomerization-Oxazolonium Ion Rearrangements. [PDF]

open access: yesChemistry
The study by Strand and co‐workers describes a concise synthesis of siphonazole B. Both oxazole units are formed from a simple propargylamine using a novel domino cycloisomerization‐rearrangement approach. Additional synthetic features include a direct aldol‐type reaction for assembling the tricyclic siphonazole core and an oxidative amidation reaction
Paulsen F   +5 more
europepmc   +2 more sources

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