کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1350771 980467 2006 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Enantioselective Michael addition of malonate esters to nitroolefins organocatalyzed by diaryl-2-pyrrolidinemethanols
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Enantioselective Michael addition of malonate esters to nitroolefins organocatalyzed by diaryl-2-pyrrolidinemethanols
چکیده انگلیسی

Bis-(3,5-dimethylphenyl)((S)-pyrrolidin-2-yl)methanol, easily prepared from l-proline, was found to be an efficient bifunctional organocatalyst, amongst the different 2-pyrrolidinemethanols tested, for the enantioselective Michael addition of malonate esters to nitroolefins. The products were isolated in good to high yields and with up to 56% ee.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Tetrahedron: Asymmetry - Volume 17, Issue 5, 6 March 2006, Pages 837–841
نویسندگان
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