Results 11 to 20 of about 17,975 (276)
Substituted Aziridines by Lithiation—Electrophile Trapping of Terminal Aziridines. [PDF]
AbstractFor Abstract see ChemInform Abstract in Full Text.
Hodgson, D, Humphreys, P, Ward, J
openaire +3 more sources
Endophytes, being the co-evolution partners of green host plants, are factories of pharmaceutically valuable novel natural products. Cochliobolus sp. APS1, an endophyte of Andrographis paniculata (Green Chiretta), produces a plethora of natural bioactive
Hiran Kanti Santra +2 more
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Aziridine derivatives involved in nucleophilic ring-opening reactions have attracted great interest, since they allow the preparation of biologically active molecules.
Valentina Verdoliva +3 more
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Recent Developments in Stereoselective Reactions of Sulfonium Ylides
This review describes advances in the literature since the mid-1990s in the area of reactions of sulfonium ylide chemistry, with particular attention paid to stereoselective examples.
Mukulesh Mondal +4 more
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Synthetic Applications of Aziridinium Ions
Nonactivated aziridine with an electron-donating group at the ring nitrogen should be activated to an aziridinium ion prior to being converted to cyclic and acyclic nitrogen-containing molecules.
Jala Ranjith, Hyun-Joon Ha
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Synthesis, structural characterization, antimicrobial and cytotoxic effects of aziridine, 2-aminoethylaziridine and azirine complexes of copper(II) and palladium(II). [PDF]
The synthesis, spectroscopic and X-ray structural characterization of copper(II) and palladium(II) complexes with aziridine ligands as 2-dimethylaziridine HNCH2CMe2 (a), the bidentate N-(2-aminoethyl)aziridines C2H4NC2H4NH2 (b) or CH2CMe2NCH2CMe2NH2 (c ...
A. Hauss +81 more
core +1 more source
The preparation of a variety of novel aziridine-γ-lactones (3) from carbohydrates is described. In contrast to aziridine-2-carboxylates, the lactones react regiospecifically at C-2 with soft nucleophiles to provide optically pure substituted β ...
Robert H. Dodd
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Coupling of 1-alkyl-2-(bromomethyl)aziridines with heteroatom-centered nucleophiles towards 2-[(heteroatom)methyl]aziridines [PDF]
The reactivity of 1-alkyl-2-(bromomethyl)aziridines with respect to different types of oxygen-, nitrogen- and sulphur-centered nucleophiles has been evaluated, pointing to the conclusion that these substrates can be applied successfully as synthetic ...
D'hooghe, Matthias, De Kimpe, Norbert
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[(2R,3R)-3-(4-Nitrophenyl)aziridin-2-yl]methanol monohydrate
The title monohydrate, C9H10N2O3·H2O, contains an aziridine ring including two contiguous stereocenters, both of which exhibit an R configuration. The methylhydroxy and nitrophenyl groups are cis-disposed about the aziridine ring.
V. Gaumet +4 more
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The reaction of a sulfur ylide with a chiral non-racemic sulfinyl imine afforded the desired aziridine in excellent yield and subsequent oxidation of the sulfinyl moiety dissolved in anhydrous dichloromethane using a 75% aqueous solution of 3 ...
David C. Forbes +4 more
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