کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5276687 | 1385563 | 2011 | 5 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Uncatalyzed reactions of α-(trihaloethylidene)nitroalkanes with push-pull enamines: a new type of ring-ring tautomerism in cyclobutane derivatives and the dramatic effect of the trihalomethyl group on the reaction pathway
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آلی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
A new type of ring-ring isomerism, which consists of the reversible transformation of cyclobutane derivatives into substituted 1,2-oxazine N-oxides was found and studied by NMR spectroscopy and X-ray diffraction analysis. The starting materials were prepared by the stereoselective reaction of α-(trifluoroethylidene)nitroalkanes, which react with ethyl β-morpholino- and β-piperidinocrotonates at the more nucleophilic α-position, whereas the reaction of α-(trichloroethylidene)nitroalkanes proceeds at the β-methyl group to give the corresponding linear products.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Tetrahedron Letters - Volume 52, Issue 44, 2 November 2011, Pages 5764-5768
Journal: Tetrahedron Letters - Volume 52, Issue 44, 2 November 2011, Pages 5764-5768
نویسندگان
Vladislav Yu. Korotaev, Alexey Yu. Barkov, Pavel A. Slepukhin, Mikhail I. Kodess, Vyacheslav Ya. Sosnovskikh,