کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1363595 | 981516 | 2005 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Thiourea-based non-nucleoside inhibitors of HIV reverse transcriptase as bifunctional organocatalysts in the asymmetric Strecker synthesis
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آلی
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چکیده انگلیسی
The potential of novel and known pyridyl thiourea derivatives (non-nucleoside inhibitors (NNI) of HIV reverse transcriptase) as bifunctional organic catalysts in the asymmetric Strecker synthesis was investigated. It was shown that incorporation of the imidazolyl moiety in place of a pyridyl group results in a new thiourea derivative that displays a much higher catalytic activity.
The potential of novel and known pyridyl thiourea derivatives (non-nucleoside inhibitors of HIV reverse transcriptase) as bifunctional organic catalysts in the asymmetric Strecker synthesis was investigated.Figure optionsDownload as PowerPoint slide
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Bioorganic & Medicinal Chemistry - Volume 13, Issue 19, 1 October 2005, Pages 5680–5685
Journal: Bioorganic & Medicinal Chemistry - Volume 13, Issue 19, 1 October 2005, Pages 5680–5685
نویسندگان
Svetlana B. Tsogoeva, Martin J. Hateley, Denis A. Yalalov, Kathrin Meindl, Christoph Weckbecker, Klaus Huthmacher,