کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1390891 | 983157 | 2007 | 5 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Enantioseparation of some chiral flavanones using microbial cyclic β-(1→3),(1→6)-glucans as novel chiral additives in capillary electrophoresis
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آلی
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![عکس صفحه اول مقاله: Enantioseparation of some chiral flavanones using microbial cyclic β-(1→3),(1→6)-glucans as novel chiral additives in capillary electrophoresis Enantioseparation of some chiral flavanones using microbial cyclic β-(1→3),(1→6)-glucans as novel chiral additives in capillary electrophoresis](/preview/png/1390891.png)
چکیده انگلیسی
Cyclic β-(1→3),(1→6)-glucans, microbial cyclooligosaccharides produced by Bradyrhizobium japonicum USDA 110, were used as novel chiral additives for the enantiomeric separation of some flavanones such as eriodictyol, homoeriodictyol, hesperetin, naringenin, and isosakuranetin in capillary electrophoresis (CE). Among the flavanones, eriodictyol was separated with the highest resolution (Rs 5.66) and selectivity factor (α 1.18) when 20 mM cyclic β-(1→3),(1→6)-glucans were added to the background electrolyte (BGE) at pH 8.3.
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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Carbohydrate Research - Volume 342, Issue 5, 9 April 2007, Pages 762–766
Journal: Carbohydrate Research - Volume 342, Issue 5, 9 April 2007, Pages 762–766
نویسندگان
Chanho Kwon, Heylin Park, Seunho Jung,