## Abstract The (N→B)phenyl[iminodiacetate‐O,O′,N]borane __1__ is stable to hydrolysis, and the fact that the N‐H proton has been shown to be more acidic than the α‐protons to the carbonyl groups has led to the syntheses of N‐substituted boron heterocycles. Thus, the reactions of compound __1__ wit
N-Germyl derivatives of sulfacetamide and ortho-(sulfonamido)phenylamines: characterization of N-[o-(N′,N′-dimethylsulfonamido)phenyl]-N-dimesitylgermaimine
✍ Scribed by C. Chazalette; A. Khallaayoun; M. Rivière-Baudet; F. El Baz
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 240 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0268-2605
- DOI
- 10.1002/aoc.406
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