Addition of di-(trimethylsilyl)phosphite to N,N′-dialkyl terephthalic schiff bases: Synthesis of 1,4-phenylene-bis- (aminomethyl)-phosphonic acids
✍ Scribed by Jarosław Lewkowski; Marek Dziȩgielewski
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 93 KB
- Volume
- 20
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20569
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✦ Synopsis
Abstract
The addition of di‐(trimethylsilyl)phosphite to N,N′‐terephthalylidene‐alkyl‐(or aryl‐)amines resulted in 1,4‐phenylene‐bis‐(N‐alkylamino‐ methyl)‐phosphonic acids in moderate yields. The stereochemical behavior of such reactions was studied, and NMR studies demonstrated that, for several examples, this reaction led to the exclusive formation of only one diastereomeric form. The investigation of the chiral salt of the acid identified the pair of enantiomers. © 2010 Wiley Periodicals, Inc. Heteroatom Chem 20:431–435, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20569
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## Abstract Terephthalic Schiff bases react with hypophosphorous acid to form 1,4‐phenylene‐bis‐__N__‐alkyl‐aminomethanephosphonous acids in moderate yields. NMR studies demonstrated that—for several examples—this reaction led to the exclusive formation of only one diastereomeric form. NMR investig
## Abstract The addition of bis‐(trimethylsilyl) phosphite to chiral imines of several aldehydes was diastereoselective. The separation of predominant diastereoisomers of a majority of formed aminophosphonic acids has been observed. Moreover, the ferrocene‐derived acid **5d** occurred in diastereos