Reaction of an imidotitanium complex, stabilized by a tridentate diamidopyridine ligand, with the methyl acetylenes MeC2Me and MeC2Ph led to C–H-activation of the substrate and subsequent C–N coupling to give azatitana-tetracycles which may be viewed as dimetallated enamines; the same compounds were obtained in reactions with the allenes Me(H)CCCH2 and Ph(H)CCCH2.
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Bashall et al. (1998) studied this question.
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