Abstract
Novel mono- and symmetrical di-N-hydroxy- and N-aminoguanidines were readily prepared from the reaction of diverse hydroxylamines or hydrazines with reagent classes di(benzotriazol-1-yl)methanimine 6, (bis-benzotriazol-1-yl- methylene)amines 8a,b, benzotriazole-1-carboxamidines 10a-i, benzotriazole-1-carboximidamides 11a,b, and N′-hydroxy-1H-1,2,3- benzotriazole-1-carboximidamide 18. The preparation is described for a variety of N-hydroxy- and N-aminoguanidines with different substitution patterns in good yields.
Original language | English (US) |
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Pages (from-to) | 6753-6758 |
Number of pages | 6 |
Journal | Journal of Organic Chemistry |
Volume | 71 |
Issue number | 18 |
DOIs | |
State | Published - Sep 1 2006 |
Externally published | Yes |
ASJC Scopus subject areas
- Organic Chemistry