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
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-
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