2013
DOI: 10.1007/s10593-013-1345-7
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Reduction of 7-R derivatives of 7H-tris[1,2,5]oxa-diazolo[3,4-b:3′,4′-d:3″,4″-f]azepine 1-oxide with furoxan ring opening. preparation of 4-R-4H-bis-[1,2,5]oxadiazolo[3,4-b:3′,4′-f]azepine-8,9-diamines

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Cited by 4 publications
(1 citation statement)
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“…At the same time, the introduction of ether bonds significantly increase the molecular flexibility, providing the compounds with plastic strength and low sensitivity, combined with energy, safety and mechanical properties. One of these compounds, bifurazano [3,4-b: 3 ,4 -f] furoxano [3 ,4 -d]oxacycloheptatriene (BFFO), with two furazan and one furoxan cycles fused into the oxacycloheptane ring, is expected to be an excellent melt-cast carrier explosive [20][21][22]. Its molecular structure is shown as Figure 1 and the energy properties are listed in Table 1 [23].…”
Section: Introductionmentioning
confidence: 99%
“…At the same time, the introduction of ether bonds significantly increase the molecular flexibility, providing the compounds with plastic strength and low sensitivity, combined with energy, safety and mechanical properties. One of these compounds, bifurazano [3,4-b: 3 ,4 -f] furoxano [3 ,4 -d]oxacycloheptatriene (BFFO), with two furazan and one furoxan cycles fused into the oxacycloheptane ring, is expected to be an excellent melt-cast carrier explosive [20][21][22]. Its molecular structure is shown as Figure 1 and the energy properties are listed in Table 1 [23].…”
Section: Introductionmentioning
confidence: 99%