1962
DOI: 10.1002/cber.19620950528
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Synthese von cytostatisch wirkenden Estern des 1‐Äthylenimino‐2‐hydroxy‐butens‐(3)

Abstract: Cytostatisch wirkende Carbonsilure-und Carbamidsiure-ester von l-kthylenimino-2-hydroxy-buten-(3) (,,Tetramin") wurden nach der Imidazolidrnethode synthetisiert.

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Cited by 17 publications
(1 citation statement)
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“…The iodide-catalyzed rearrangement of the formerly mentioned compounds provides a method for preparing the tetrahydroimidazoimidazole system: Ethyleneimine reacts with epoxides to form hydroxyalkylated products, eg, N-(β-hydroxyethylaziridine) [1072-52-2]. The epoxide component is frequently used in substoichiometric amount in order to prevent multiple alkoxylation (180)(181)(182)(183)(184)(185)(186)(187)(188)(189)(190). Ethyleneimine and episulfides react to give complex product mixtures, since the 1-(2mercaptoethyl)aziridine produced initially can easily react further with both reactants (191,192).…”
Section: Reaction Of Cyanuric Chloride [108-77-0] With Ethyleneimine mentioning
confidence: 99%
“…The iodide-catalyzed rearrangement of the formerly mentioned compounds provides a method for preparing the tetrahydroimidazoimidazole system: Ethyleneimine reacts with epoxides to form hydroxyalkylated products, eg, N-(β-hydroxyethylaziridine) [1072-52-2]. The epoxide component is frequently used in substoichiometric amount in order to prevent multiple alkoxylation (180)(181)(182)(183)(184)(185)(186)(187)(188)(189)(190). Ethyleneimine and episulfides react to give complex product mixtures, since the 1-(2mercaptoethyl)aziridine produced initially can easily react further with both reactants (191,192).…”
Section: Reaction Of Cyanuric Chloride [108-77-0] With Ethyleneimine mentioning
confidence: 99%