Differential Effects of Nitrogen-Substitution in 5- and 6-Membered Aromatic Motifs
The replacement of carbon with nitrogen can affect the aromaticity of organic rings. Nucleus-independent chemical shift (NICS) calculations at the center of the aromatic π-systems reveal that incorporating nitrogen into 5-membered heteroaromatic dienes has only a small influence on aromaticity. In c...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley,
2021-02-19T22:57:35Z.
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| Online Access: | Get fulltext |
| Summary: | The replacement of carbon with nitrogen can affect the aromaticity of organic rings. Nucleus-independent chemical shift (NICS) calculations at the center of the aromatic π-systems reveal that incorporating nitrogen into 5-membered heteroaromatic dienes has only a small influence on aromaticity. In contrast, each nitrogen incorporated into benzene results in a sequential and substantial loss of aromaticity. The contrasting effects of nitrogen substitution in 5-membered dienes and benzene are reflected in their Diels-Alder reactivities as dienes. 1,2-Diazine experiences a 1011-fold increase in reactivity upon nitrogen substitution at the 4- and 5-positions, whereas a 5-membered heteroaromatic diene, furan, experiences a comparatively incidental 102-fold increase in reactivity upon nitrogen substitution at the 3- and 4-positions. ©2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim NIH (F32 GM137543) NIH Grant (R01 GM044783) NSF Grant (ACI-1548562) |
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