期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2011, 期 5, 页码 983-992出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201001365
关键词
Density functional calculations; Hetero-Diels-Alder reactions; Heterocycles; Oxazines; Triazines
资金
- Justus Liebig University (JLU) of Giessen
- University of Queensland
We present an analysis of the well-known normal-and inverse-electron-demand hetero-Diels-Alder reaction involving 1,2,4-triazine, 1,3-oxazin-6-one, and 1,4-oxazin-2-one, with alkenes and alkynes, utilizing density functional theory (DFT) at the SCS-MP2/cc-pVDZ//B3LYP/6-31G(d) level to establish a theoretical status quo for synthetic practioners regarding the relative reactivities and stereochemical outcomes for these useful heterocycles. The results suggest that in the unsubstituted cases 1,2,4-triazine is less reactive in comparison to 1,3-oxazin-6-one and 1,4-oxazin-2-one for both reaction modes, whereas the cycloaddition regioselectivities depend largely on the diene. For example, 1,3-oxazin-6-one leads to kinetic meta isomers, in comparison to 1,2,4-triazine and 1,4-oxazin-2-one, which give rise to para isomers.
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