Results 11 to 20 of about 5,622 (203)

Dimerization and Isomerization Reactions of α-Lithiated Terminal Aziridines

open access: yes, 2016
The scope of dimerization and isomerization reactions of α-lithiated terminal aziridines is detailed. Regio- and stereoselective deprotonation of simple terminal aziridines with lithium 2,2,6,6-tetramethylpiperidide (LTMP) or lithium dicyclohexylamide ...
David M. Hodgson (692207)   +4 more
core   +8 more sources

Copper-Catalyzed Ring-Opening Reactions of Alkyl Aziridines with B2pin2: Experimental and Computational Studies

open access: yesMolecules, 2021
The possibility to form new C–B bonds with aziridines using diboron derivatives continues to be a particularly challenging field in view of the direct preparation of functionalized β-aminoboronates, which are important compounds in drug discovery, being ...
Lucilla Favero   +6 more
doaj   +1 more source

Cooperative chalcogen bonding interactions in confined sites activate aziridines

open access: yesNature Communications, 2022
The activation of aziridines is typically achieved via reaction with strong Lewis acids or transition metals. Here, the authors report that cooperative Se ∙ ∙∙O and Se ∙ ∙∙N noncovalent interactions can activate sulfonyl-protected aziridines, which ...
Haofu Zhu, Pan-Pan Zhou, Yao Wang
doaj   +1 more source

Preface to “Aziridine Chemistry” [PDF]

open access: yesMolecules, 2021
Aziridine is a nitrogen-containing three-membered ring with similar ring strain energy as other three-membered ring compounds, including cyclopropane and oxirane [...]
openaire   +3 more sources

Regioselective and Stereodivergent Synthesis of Enantiomerically Pure Vic-Diamines from Chiral β-Amino Alcohols with 2-Pyridyl and 6-(2,2′-Bipyridyl) Moieties

open access: yesMolecules, 2020
In this report, we describe the synthetic elaboration of the easily available enantiomerically pure β-amino alcohols. Attempted direct substitution of the hydroxyl group by azido-functionality in the Mitsunobu reaction with hydrazoic acid was ...
Marzena Wosińska-Hrydczuk   +2 more
doaj   +1 more source

The Synthesis of (2R)-Aziridine-2-carboxylic Acid Containing Dipeptides

open access: yesActa Chimica Slovenica, 2022
Optimized conditions for the synthesis of fully deprotected (2R)-aziridine containing dipeptides are described. Preparation of fully protected N- and C- terminal aziridine containing dipeptides was found to be straightforward and high yielding for the ...
Samo Kuzmič, Martina Hrast, Rok Frlan
doaj   +1 more source

Triethylamine-Promoted Oxidative Cyclodimerization of 2H-Azirine-2-carboxylates to Pyrimidine-4,6-dicarboxylates: Experimental and DFT Study

open access: yesMolecules, 2023
An unprecedented oxidative cyclodimerization reaction of 2H-azirine-2-carboxylates to pyrimidine-4,6-dicarboxylates under heating with triethylamine in air is described. In this reaction, one azirine molecule undergoes formal cleavage across the C-C bond
Timofei N. Zakharov   +4 more
doaj   +1 more source

Access to 2-Fluorinated Aziridine-2-phosphonates from α,α-Halofluorinated β-Iminophosphonates—Spectroscopic and Theoretical Studies

open access: yesMolecules, 2023
The efficient one-pot halofluorination of a β-enaminophosphonate/β-iminophosphonate tautomeric mixture resulting in α,α-halofluorinated β-iminophosphonates is reported.
Mateusz Klarek   +4 more
doaj   +1 more source

Nickel/biimidazole-catalyzed electrochemical enantioselective reductive cross-coupling of aryl aziridines with aryl iodides

open access: yesNature Communications, 2023
Here, we report an asymmetric electrochemical organonickel-catalyzed reductive cross-coupling of aryl aziridines with aryl iodides in an undivided cell, affording β-phenethylamines in good to excellent enantioselectivity with broad functional group ...
Yun-Zhao Wang   +7 more
doaj   +1 more source

A Mild and Efficient Method for the Syntheses and Regioselective Ring-Opening of Aziridines

open access: yesSynOpen, 2017
We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an effective reagent in the presence of NH2OH·HCl and NaIO4.
Nirnita Chakraborty Ghosal   +5 more
doaj   +1 more source

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