1999
DOI: 10.1002/(sici)1099-0690(199903)1999:3<661::aid-ejoc661>3.3.co;2-m
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New Type of Skipped Oligoaziridines: Synthesis of New Fatty AcidDerivatives Containing Aziridine Functions

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Cited by 10 publications
(11 citation statements)
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(9 reference statements)
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“…[26,27] Scheme 3. [27] The aziridines 22 and the episulfides 23, [28] the latter being accessible from the epoxides 14 b and 15 b (Scheme 4), are interesting intermediates in the synthesis of heterocyclic and highly functionalized fatty compounds. [26] Methyl di-and triepiminooctadecanoates 22 b and 22 c can be synthesized in a similar manner from the methyl di-and triepoxyoctadecanoates 15 b and 16 b.…”
Section: Follow-up Reactions Of Epoxides To Aziridines and Episulfidesmentioning
confidence: 99%
“…[26,27] Scheme 3. [27] The aziridines 22 and the episulfides 23, [28] the latter being accessible from the epoxides 14 b and 15 b (Scheme 4), are interesting intermediates in the synthesis of heterocyclic and highly functionalized fatty compounds. [26] Methyl di-and triepiminooctadecanoates 22 b and 22 c can be synthesized in a similar manner from the methyl di-and triepoxyoctadecanoates 15 b and 16 b.…”
Section: Follow-up Reactions Of Epoxides To Aziridines and Episulfidesmentioning
confidence: 99%
“…Aziridines that contain fatty acids have demonstrated promising biological properties and are good candidates for further functionalization; consequently, several groups have reported the synthesis of fatty‐acid‐derived aziridines . Jurgen O. Metzger and Sandra Fürmeier synthesized bis‐ and tris‐aziridines from long‐chain unsaturated fatty acids, such as linoleic and linolenic acid . Initially, they tried previously reported approaches, as shown in Scheme a, but the first two methods were unsuccessful.…”
Section: Nh‐aziridination Of Fatty Acidsmentioning
confidence: 99%
“…[26,27] Die Aziridine 22 und ebenso die aus den Epoxiden 14 b und 15 b zugänglichen Episulfide 23 [28] (Schema 4) sind interessante Zwischenstufen zur Synthese heterocyclischer und hochfunktionalisierter Fettstoffe. [27] Schema 4. Synthese von Epiminooctadecansäuremethylester 22 a aus Epoxyoctadecansäuremethylester 14 b: a) NaN 3 , NH 4 Cl, EtOH, H 2 O; b) Ph 3 P, THF.…”
Section: Folgereaktionen Von Epoxiden Zu Aziridinen Und Episulfidenunclassified