Synthesis of aziridines by visible-light induced decarboxylative cyclization of N-aryl glycines and diazo compounds
A visible-light induced decarboxylative aza-Darzens reaction between N-aryl glycines and diazo compounds was developed, which affords various mono-substituted aziridines in good yields.
A new synthesis of aziridine-2-carboxylates: Reaction of hexahydro- 1,3,5-triazines or N-methoxymethylanilines with alkyl diazoacetates in the presence of Lewis acid
Aziridine-2-carboxylates were prepared from the reaction of hexahydro- 1,3,5-triazines or N-methoxymethylanilines with alkyl diazoacetates in the presence of Lewis acid catalyst in high yield.
Ha, Hyun-Joon,Suh, Jang-Min,Kang, Kyung-Ho,Ahn, Young-Gil,Han, Oksoo
p. 851 - 858
(2007/10/03)
A new synthesis of aziridine-2-carboxylates by reaction of hexahydro-1,3,5-triazines with alkyldiazoacetates in the presence of tin(IV) chloride
Aziridine-2-carboxylates were prepared from the reaction of hexahydro-1,3,5-triazines with alkyldiazoacetates in the presence of Lewis acid catalyst in high yield.
Ha, Hyun-Joon,Kang, Kyung-Ho,Suh, Jang-Min,Ahn, Young-Gil
p. 7069 - 7070
(2007/10/03)
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