کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
68431 48514 2006 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Efficient catalytic synthesis of optically pure 1,2-azido alcohols through enantioselective epoxide ring opening with HN3
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Efficient catalytic synthesis of optically pure 1,2-azido alcohols through enantioselective epoxide ring opening with HN3
چکیده انگلیسی

Chiral binuclear Co(salen) complexes bearing Lewis acid of group 13 metal chlorides show very high catalytic activity and enantioselectivity for the ring opening of epoxides using HN3 as azide source. It provides a facile and practical synthetic route to a wide range of chiral nonracemic 1,2-azido alcohols and related compounds in one-pot synthesis with excellent selectivity (92.0–99.6% e.e.) under mild conditions. The presence of Lewis acid of group 13 shows a strong synergistic effect.

Inactive Co(salen) complexes are easily activated by the Lewis acid of group 13 metal chlorides as a result of formation of heterometallic complexes. These complexes show very high catalytic activity for the asymmetric ring opening of epoxides with HN3. Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Catalysis A: Chemical - Volume 259, Issues 1–2, 15 November 2006, Pages 116–120
نویسندگان
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