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N-O acyl migration in the N-benzoyl derivatives of cis- trans-2-aminomethylcyclopentanol and cis- and trans-2-hydroxymethylcyclopentylamine

✍ Scribed by G. Bernáth; K.L. Láng; Gy. Göndös; P. Márai; K. Kovács


Publisher
Elsevier Science
Year
1968
Tongue
French
Weight
200 KB
Volume
9
Category
Article
ISSN
0040-4039

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✦ Synopsis


In a previous Letter 111 the N-O acyl migration of cis-and trans-2--aminomethylcyclohexanol and cis-and trans-2-hydroxymetbylcyclohexylamine derivatives was reported. The present coamnznication deals with the stereospecific synthesis of the analogous cyclopentane derivatives, as well as the examination of the kinetics of their N-O acyl migration reaction. The stereospecific synthesis of cis-and trans-2-aminomethylcyclopentanol and cis-and trans-2-hydroxymethylcyclopentylamine was achiwed by LiAlH4 reduction of G-and trans-2-hydroxycyclopentanecarboxamide and e-


📜 SIMILAR VOLUMES


N → O acyl migration in cis and trans-2-
✍ G. Bernáth; K. Kovács; K.L. Láng 📂 Article 📅 1968 🏛 Elsevier Science 🌐 French ⚖ 207 KB

I&any papers, including kinetical studies, have been published oonoerning N -c 0 aoyl migrations in 1,2-aminoalcohols /e.g. 1, 2/ and in alicyolic systems /e.g. 3/; details of the mechanism are still under investigation /4/. The similar reactions of 1,3\_aninoalcohols /5-T/ and 1,4\_nninoalcohols /8