## 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
Syntheses of (N → B)phenyl[N-alkylaminodiacetate-O,O′,N]boranes
✍ Scribed by Teresa Mancilla; Lourdes Carrillo; Ma.de la Paz Reducindo
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 725 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0277-5387
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Single-crystal X-ray study T = 571 K Mean '(C±C) = 0.012 A Ê R factor = 0.047 wR factor = 0.123 Data-to-parameter ratio = 13.1 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.