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PIDA-Mediated Synthesis of Symmetrical 1,2,4,5-Tetrazine Using N-Tosylhydrazones
- Singhal, Rakshanda;
- Mehra, Manish Kumar;
- Malik, Babita;
- Pilania, Meenakshi
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0초록
A rapid and effective method for the preparation of 3,6-disubstituted-1,2,4,5-tetrazines from N-tosylhydrazones has been developed using phenyliodine(III) diacetate as an oxidant and cesium carbonate (Cs2CO3) as a base. The reaction completes in a single step under transition-metal-free conditions through an oxidative C-N bond-formation approach. This developed method offers numerous advantages, including a short reaction time (15 min), operational simplicity, mild conditions, and moderate to high product yields. In general, this methodology offers a practical and useful approach for synthesizing 1,2,4,5-tetrazine scaffolds, which are highly valuable in both synthetic and medicinal chemistry.
키워드
N-Tosylhydrazone; Hypervalent iodine; Phenyliodine(III) diacetate; 1,2,4,5-Tetrazine; Aromatization; ONE-POT SYNTHESIS; BOND FORMATION; ANTITUMOR-ACTIVITY; DERIVATIVES; QUINOXALINONES; BENZIMIDAZOLE; REARRANGEMENT; CYCLIZATION; TETRAZINES; CHEMISTRY
- 제목
- PIDA-Mediated Synthesis of Symmetrical 1,2,4,5-Tetrazine Using N-Tosylhydrazones
- 저자
- Singhal, Rakshanda; Mehra, Manish Kumar; Malik, Babita; Pilania, Meenakshi
- 발행일
- 2026-03
- 유형
- Article; Early Access
- 저널명
- Synthesis