1985
DOI: 10.1002/cber.19851180514
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2‐Azaallenium salts from the reaction of 1‐oxa‐3‐azabutatrienium salts with cyanamides and carbodiimides

Abstract: 1‐Oxa‐3‐azabutatrienium salts 2 react with disubstituted cyanamides under [2 + 2 + 2] cycloaddition affording the 2‐(alkylideneamino)‐4,6‐diamino‐1,3,5‐oxadiazinium salts 7a – o, which can be regarded as oxy‐substituted 2‐azaallenium salts. Addition of methanol leads to the oxadiazinium salts 8a, d, p. From 2n and dimethylcyanamide the 2‐azaallenium salt 11 was obtained, which must be formed by an [1,5] isocyanatotropic rearrangement. Most butatrienium salts 2 react with two equivalents of carbodiimides R1  N… Show more

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Cited by 23 publications
(2 citation statements)
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“…In (1) bond distances in the cationic 1,3,5-oxadiazinium ring agree well with those previously reported (Rushton, Schwalbe & Stevens, 1983;A1-Talib, Jochims, Zsolnai & Huttner, 1985;Hartung, Beyer, Guti6rrez-Puebla, Fernandez & Olk, 1992). The oxadiazinium ring is planar [maximum deviation -0.045 A for C(4)], as is the phenyl ring, and the angle between these rings is 2.6 °.…”
Section: Commentsupporting
confidence: 90%
“…In (1) bond distances in the cationic 1,3,5-oxadiazinium ring agree well with those previously reported (Rushton, Schwalbe & Stevens, 1983;A1-Talib, Jochims, Zsolnai & Huttner, 1985;Hartung, Beyer, Guti6rrez-Puebla, Fernandez & Olk, 1992). The oxadiazinium ring is planar [maximum deviation -0.045 A for C(4)], as is the phenyl ring, and the angle between these rings is 2.6 °.…”
Section: Commentsupporting
confidence: 90%
“…[C,,H 9,21.4,22.5,22.7,23.2,23.5,CH,41.3,CH 51.5,55.3,58.7 CH 51. 8,55.3,58.6,59.3,CCI,90.8,C = N 135.3,154.9, C = O 160.9. 5,21.3,21.8,22.2,22.3,23.2,23.6,CH 51.1,54.6,55.3,58.3,C = O 172.0,C = N 157.4,136.2,phenyl 143.2,130.3,127 Reaction of Cyclohexylisopropylcarbodiimide with Acetylium Hexachloroantirnonate: Formation of 13r: As described for 13a from cyclohexylisopropylcarbodiimide (2.50 g, 15.05 mmol).…”
Section: Experimental Partmentioning
confidence: 98%