29Si NMR spectra of a series of tert-butyldimethylsilyl derivatives of simple alcohols were measured under standard conditions in chloroform-d. The chemical shifts are linearly related to those in analogous trimethylsilyl derivatives. The correlation is very good (r = 0.998, n = 24) but signiÐcantly
29Si and 13C NMR spectra of tert-butyldimethylsilyl derivatives of amino acids
✍ Scribed by Roman Kubec; Jan Velíšek; Magdalena Kvíčalová; Jan Čermák; Jan Schraml
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 245 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^29^Si and ^13^C NMR chemical shifts are reported for tert‐butyldimethylsilyl (TBDMS) derivatives of ten common amino acids. The ^29^Si chemical shifts of TBDMS derivatives of various functionalities encountered fall into distinct spectral regions. The ^29^Si chemical shifts correlate linearly (r = 0.999) with the ^29^Si shifts reported earlier for the trimethylsilyl (TMS) derivatives of the same amino acids, the ^29^Si chemical shift values in the TBDMS derivatives being larger than those in the TMS derivatives (in SiN groups this downfiled shift varies between 3.8 and 5.8 ppm and in SiO groups between 1.4 and 1.7 ppm).
📜 SIMILAR VOLUMES
Twelve para-and meta-substituted benzhydroxamic acids were subjected to exhaustive silylation with N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide (with 1% of tert-butyldimethylsilyl chloride as a catalyst). In all cases only one product was isolated. According to the assigned NMR spectra ( 1
## Abstract The ^29^Si and ^13^C NMR chemical shifts are reported for trimethylsilyl derivatives of 25 amino acids, the majority of which occur naturally as protein constituents of foodstuffs. The ^29^Si chemical shifts in trimethylsilyl esters of amino acids roughly correlate linearly with the p__
Trimethylsilyl and tert-butyldimethylsilyl derivatives of naturally occurring purines and pyrimidines and also other closely related model compounds were prepared and their 29Si NMR spectra measured. Only the chemical shifts of the SiÈNHÈ moiety could be assigned experimentally (i.e. exactly) ; the
13C chemical shifts and ,'P,13C coupling constants are reported for 20 aminoalkylphosphonic acids and two phosphonic acids. The substituent-induced chemical shifts of the phosphonate group were calculated and their non-additivity in 1 -aminoalkylphosphonic acids was observed. Two stable conformers o