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Synthesis of orthogonally protected 1,2-diaminopropanoic acids by ring-opening of 3-unsubstituted N-activated aziridine 2-carboxylates with para-methoxybenzylamine: a study of the regioselectivity of the reaction

✍ Scribed by O’Brien, Keith; Kelleher, Fintan

Book ID
121349799
Publisher
Elsevier Science
Year
2013
Tongue
French
Weight
530 KB
Volume
54
Category
Article
ISSN
0040-4039

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A new synthesis of aziridine-2-carboxyla
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
✍ Hyun-Joon Ha; Jang-Min Suh; Kyung-Ho Kang; Young-Gil Ahn; Oksoo Han 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 474 KB

4b~t: Aziridine-2-carboxylates were prepared from the reaction of hexahydro-l,3,5-triazines or Nmethoxymethylanilines with alkyl diazeacetates in the presence of Lewis acid catalyst in high yield.