Line narrowing of amide proton resonances in 2D NMR spectra of proteins
Line narrowing of amide proton resonances in 2D NMR spectra of proteins
复制标题
蛋白质二维 NMR 谱中酰胺质子共振谱线的窄化
DOI:
10.1021/ja00183a082
复制
发表时间:
1989
影响因子:
15
通讯作者:
D. Torchia
中科院分区:
文献类型:
--
作者:
A. Bax;L. Kay;S. W. Sparks;D. Torchia
(14) (a) The rates of alkyl radical addition to mono-substituted alkenes depend on the nature of the alkene substituents. For example, the addition rates to CH2=CHCOCH, are normally double those to CHI=CHCO2CH3 (ref 14b). Importantly, simple a-amino alkyl radicals are electron rich (high-energy SOMO) and thus should add to electron poor olefins more efficiently. This should be contrasted to the chemistry of a-amido alkyl radicals which add intramolecularly to simple alkene groupings (ref 14c). (b) Giese, B. Angew. Chem., In t . Ed. Engl. 1983, 764, 763 and references therein. (c) Hart, D. J . ; Tasi, Y . M. J . Am. Chem. SOC. 1982, 104, 1430. Burnett, D. A.; Choi, J . K.; Hart, D. J.; Tsai, Y . M. Ibid. 1984, 106, 8201. (1 5 ) For example, the comparative lack of and modest stereoselectivity of the respective direct and SET-sensitized photocyclizations of 9 needs to be addressed. Line Narrowing of Amide Proton Resonances in 2D NMR Spectra of Proteins