Results 91 to 100 of about 7,765 (231)
Azirydyna jest bezbarwną, lotną, wysoce łatwopalną cieczą o zapachu podobnym do amonia-ku. Jest stosowana do produkcji trietylenomelaminy i 2-azirydynyloetanolu oraz jako monomer do produkcji polimerów (głównie polietylenoiminy).
Zaborowska, A. +2 more
core
The utility of aziridine as a clickable moiety for post-modification of polydimethylsiloxane is demonstrated.
Hyun Kyung Moon +2 more
core +1 more source
Salen–scandium(III) complex-catalyzed asymmetric (3 + 2) annulation of aziridines and aldehydes
Oxazolidine is one of the crucial structural moieties of biologically active compounds. A salen–scandium triflate complex-catalyzed asymmetric (3 + 2) annulation of dialkyl 1-sulfonylaziridine-2,2-dicarboxylates and aldehydes generated optically active ...
Linqiang Wang, Jiaxi Xu
doaj +1 more source
Metal-free one-pot synthesis of 2-substituted and 2,3-disubstituted morpholines from aziridines
The metal-free synthesis of 2-substituted and 2,3-disubstituted morpholines through a one-pot strategy is described. A simple and inexpensive ammonium persulfate salt enables the reaction of aziridines with halogenated alcohols to proceed via an SN2-type
Hongnan Sun +4 more
doaj +1 more source
An hydroxypropyl-aziridine-containing side chain is attached to an oxonaphthalene-annelated pyrrole in expectation of DNA alkylating properties. The cytotoxicity is evaluated against two cell lines, KB-31 and KB-8511, respectively.
Christiane Puschmann, Helmut Spreitzer
doaj +1 more source
Aziridine – a determination method
Metoda polega na chemisorpcji zawartej w powietrzu azirydyny na żywicy XAD-2 z naniesionym izo-tiocyjanianem 1-naftylu, desorpcji N,N-dimetyloformamidem i analizie otrzymanego roztworu metodą wysokosprawnej chromatografii cieczowej.The method is based on
Jeżewska, A.
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Aziridine−Allylsilane-Mediated Total Synthesis of (−)-Yohimbane
A total asymmetric synthesis of (−)-yohimbane and ent-alloyohimbane is reported. The synthesis utilizes a novel aziridine−allylsilane cyclization reaction as a key step in the synthesis.
Punit P. Seth (628027) +1 more
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Jaunu C-C saišu veidošana aziridīn-2-karbonskābes atvasinājumos, saglabājot trīslocekļu slāpekļa heterociklus. Štrumfs B., zinātniskais vadītājs Dr. ķīm. Trapencieris P. Promocijas darbs, 165 lappuses, 6 attēli, 3 tabulas, 100 literatūras avoti. Latviešu
Štrumfs, Boriss, Boriss Štrumfs
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Efficient, regioselective ring-opening of activated aziridine-2-carboxylates with [18F]fluoride
Aziridines can undergo a range of ring-opening reactions with nucleophiles. The regio- and stereochemistry of the products depend on the substituents on the aziridine. Aziridine ring-opening reactions have rarely been used in radiosynthesis.
Hansen, Paul Robert +3 more
core +1 more source
Functionalised Enones as Starting Materials for the Construction of Aziridine Scaffolds
alpha-Substituted beta-keto esters have been transformed by means of a straightforward procedure into aziridine-1,2-dicarboxylates, which have been efficiently converted into alkenyl aziridine-1,2-dicarboxylates through Wittig olefination reaction.
MORREALE, Alberto +3 more
core +1 more source

