2012
DOI: 10.3184/174751912x13305927311260
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Synthesis and Structure Analysis of N1,N4-di-tert-Butyl-3,6-Dimethyl-1,4-Dihydro-1,2,4,5-Tetrazine-1,4-Dicarboxamide

Abstract: N 1 ,N 4 -Di-tert-butyl-3,6-dimethyl-1,4-dihydro-1,2,4,5-tetrazine-1,4-dicarboxamide was prepared from 3,6-dimethyl-1,6dihydro-1,2,4,5-tetrazine, and its structure was confirmed by single-crystal X-ray diffraction. This reaction yields the 1,4-dicarboxamide derivative rather than the 1,2-dicarboxamide derivative. The central six-member ring of the title compound has a boat conformation and therefore, is not homoaromatic. * Correspondent.

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Cited by 2 publications
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“…1,2,4,5-Tetrazine derivatives have been widely used in medicinal chemistry and organic synthetic chemistry. [1][2][3][4][5][6][7] Dihydro-1,2,4,5-tetrazine has four isomers, namely 1,2-, 1,4-, 1,6-and 3,6-dihydro-1,2,4,5-tetrazine. Homoaromatic structures have been demonstrated by X-ray diffraction in the 1,6-dihydro structures.…”
mentioning
confidence: 99%
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“…1,2,4,5-Tetrazine derivatives have been widely used in medicinal chemistry and organic synthetic chemistry. [1][2][3][4][5][6][7] Dihydro-1,2,4,5-tetrazine has four isomers, namely 1,2-, 1,4-, 1,6-and 3,6-dihydro-1,2,4,5-tetrazine. Homoaromatic structures have been demonstrated by X-ray diffraction in the 1,6-dihydro structures.…”
mentioning
confidence: 99%
“…8 But there is still some doubt as to whether 1,4dihydro structures have homoaromaticity. For instance, X-ray diffraction was reported to show that several 1,4-dihydro-1,2,4,5-tetrazine derivatives have an obvious boat conformation without a homoaromatic structure, [4][5][6][7] and 3,6-bis(4-chlorobenzyl)-1,4-dihydro-1,2,4,5-tetrazine have an obvious chair conformation without a homoaromatic structure 9 . But 1,3,4,6tetramethyl-1,4-dihydro-1,2,4,5-tetrazine was analysed by X-ray diffraction and Bemis et al 10 deemed that this potentially antiaromatic or homoaromatic ring system had a flattened boat conformation with both N-methyls in equatorial positions.…”
mentioning
confidence: 99%