Results 11 to 20 of about 2,054 (167)
Nature 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
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A Mild and Efficient Method for the Syntheses and Regioselective Ring-Opening of Aziridines
SynOpen, 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
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Molecules, 2022 A type of MCM-41 supported dicationic imidazolium ionic liquid nanocatalyst has been synthesized and found to be competent for the synthesis of 2-oxazolidinones through the sustainable chemical conversion of CO2 with aziridines.
Yulin Hu, Lili Yang, Xiaobing Liu
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Preface to “Aziridine Chemistry” [PDF]
Molecules, 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
Asymmetric synthesis of CF2-functionalized aziridines by combined strong Brønsted acid catalysis
Beilstein Journal of Organic Chemistry, 2020 A diastereo- and enantioselective approach to access chiral CF2-functionalized aziridines from difluorodiazoethyl phenyl sulfone (PhSO2CF2CHN2) and in situ-formed aldimines is described.
Xing-Fa Tan, Fa-Guang Zhang, Jun-An Ma
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Pd-Catalyzed Cycloaddition of Bicyclic Aziridine with Isocyanates
Medical Sciences Forum, 2022 Nitrogen-containing heterocycles can have several applications in the pharmaceutical industry since they contain a wide spectrum of biological activities. Imidazolidinones have shown activity against leukemia, lung cancer, and metabolic disorders.
Mariana Crespo Monteiro +2 more
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Preparation and ring-opening reactions of N-diphenylphosphinyl vinyl aziridines
Beilstein Journal of Organic Chemistry, 2013 Predominantly (E)-N-diphenylphosphinyl vinyl aziridines are prepared by a reaction of N-diphenylphosphinyl imines with α-bromoallyllithium in the presence of freshly fused ZnCl2.
Ashley N. Jarvis +3 more
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Beilstein Journal of Organic Chemistry, 2021 The reported flow-batch approach enables the easy preparation of 2H-azirines and their stereoselective transformation into highly functionalized NH-aziridines, starting from vinyl azides and organolithium compounds.
Michael Andresini +2 more
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Organocatalyzed enantioselective desymmetrization of aziridines and epoxides
Beilstein Journal of Organic Chemistry, 2013 Enantioselective desymmetrization of meso-aziridines and meso-epoxides with various nucleophiles by organocatalysis has emerged as a cutting-edge approach in recent years.
Ping-An Wang
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Química Nova, 2007 This article surveys a selection of the most recent advances in aziridine synthesis. Novel synthetic methods and new insights into existing methodologies for the selective construction of the title compounds reported in the past decade are discussed in ...
Tula Beck Bisol, Marcus Mandolesi Sá
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