کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5221591 | 1383424 | 2010 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Mechanistic elucidation of ketenimine-butynoate cycloaddition reaction: role of biradical intermediates in isotopomeric purity of benzyl (1,1a,6,6a-13C4)-6-methyl anthranilic ester
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آلی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Thermal Diels-Alder reaction of vinyl ketenimines with 13C-labeled 2-butynoate, efficiently prepared from 13C4-acetoacetate via the enol triflate, rendered at 160 °C the corresponding methylanthranilic ester isotopomerically pure. However, when the reaction was run at 100 °C, 7% of isotope exchange between C6a and C5 was observed. This result is explained through a base-like catalyzed isomerization of the alkyne to the corresponding allene. Combined DFT and coupled-cluster computations show the feasibility of this mechanistic proposal. Better agreement between DFT and coupled-cluster activation and reaction energies is observed for the meta-GGA MPWB1K functional as compared to previous B3LYP results.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Tetrahedron - Volume 66, Issue 21, 22 May 2010, Pages 3855-3860
Journal: Tetrahedron - Volume 66, Issue 21, 22 May 2010, Pages 3855-3860
نویسندگان
Armando Navarro-Vázquez, José-Lorenzo Alonso-Gómez, Johan Lugtenburg, MarÃa-Magdalena Cid,