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Isoquinolinium N-Arylimides and Some Cycloadditions to Heterocumulenes

✍ Scribed by Klaus Bast; Matthias Behrens; Toni Durst; Rudolf Grashey; Rolf Huisgen; Reinhard Schiffer; Robert Temme

Book ID
102657815
Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
507 KB
Volume
1998
Category
Article
ISSN
1434-193X

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✦ Synopsis

The red isoquinolinium N-arylimides 19؊23 are azomethine mer. Generated by deprotonation of 11؊13, the N-arylimides 19؊21 undergo in situ cycloadditions to carbon disulfide, imines of which the C=N bond is part of an aromatic ring. The N-(4-nitrophenyl)imide 22 and the N-(2-pyridyl)imide 23 phenyl isocyanate, phenyl isothiocyanate, and diphenylketene. The storable CS 2 adduct 29 offers a neutral source of were obtained crystalline; in solution the latter equilibrates with the hexahydrotetrazine 24 as its dimer. The N-phenyl-the N-phenylimide 19, since a cycloreversion equilibrium is established in solution. imide 19 is not stable; an isolated solid appears to be a tetra-

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