Abstract
Stable and isolable 8:1 electrons antiaromatic compounds, 2-vinyl and 2,5-divinyl substituted 1,4-diazapentalenes were synthesized via an oxidation reaction of correspondingly substituted 1,4-dihydro-3,6-di-tert-butylpyrrolo[3,2-b]pyrroles which were prepared by an electrophilic addtion reaction of dimethyl acetylenedicarboxylate (DMAD).
| Original language | English |
|---|---|
| Pages (from-to) | 433-436 |
| Number of pages | 4 |
| Journal | Heterocycles |
| Volume | 48 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Jan 1 1998 |
ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry
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Cite this
Satake, K., Nakogc, D., & Kimura, M. (1998). Stable antiaromatic 1,4-diazapentalenes: synthesis and oxidation reaction of 2-vinyl- and 2,5-divinyl-1,4-dihydropyrrolo[3,2-b]pyrrole derivatives. Heterocycles, 48(3), 433-436. https://doi.org/10.3987/COM-97-8071