Comprehensive Heterocyclic Chemistry III 2008
DOI: 10.1016/b978-008044992-0.01012-9
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Bicyclic 5-6 Systems with One Bridgehead (Ring Junction) Nitrogen Atom: Two Extra Heteroatoms 1:1

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Cited by 4 publications
(8 citation statements)
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“…Pyrazoles can act as weak bases or acids, with possible strength highly dependent on the nature of their substituent groups. The other three positions in the ring permit structural variants starting from the appropriate precursors or using post-functionalization reactions once the pyrazole ring is formed [1][2][3][4][5]; these variations give the pyrazoles diverse and valuable synthetical, biological, and photophysical properties; indeed, more complex structures with various relevant examples can be formed from them (Figure 1) [1][2][3][4][5][6][7][8][9].…”
Section: Introductionmentioning
confidence: 99%
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“…Pyrazoles can act as weak bases or acids, with possible strength highly dependent on the nature of their substituent groups. The other three positions in the ring permit structural variants starting from the appropriate precursors or using post-functionalization reactions once the pyrazole ring is formed [1][2][3][4][5]; these variations give the pyrazoles diverse and valuable synthetical, biological, and photophysical properties; indeed, more complex structures with various relevant examples can be formed from them (Figure 1) [1][2][3][4][5][6][7][8][9].…”
Section: Introductionmentioning
confidence: 99%
“…Some fused pyrazoles also have demonstrated different biological activities, exceptional photophysical properties, and high synthetical versatility that allow the obtention of industrially and pharmaceutically crucial chemicals [1][2][3][4][5][6][7][8][9]; thus, synthesizing pyrazole derivatives efficiently and selectively is an important area of organic chemistry. For instance, pyrazoles have biological activities in many specific areas, such as anticancer, antibacterial, antifungal, antioxidant, and anti-inflammatory, among others [1,8].…”
Section: Introductionmentioning
confidence: 99%
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“…Regardless, innovative synthesis methods still emerge that offer creative ways to modify established ones. Notably, the main synthesis route of pyrazolo[1,5-a]pyrimidines allows versatile structural modifications at positions 2, 3, 5, 6, and 7 via the cyclocondensation reaction of 1,3-biselectrophilic compounds with NH-3-aminopyrazoles as 1,3-bisnucleophilic systems ( Figure 1 b) [ 1 , 2 , 3 , 4 , 5 , 6 , 24 , 25 ].…”
Section: Synthesis and Functionalizationmentioning
confidence: 99%