67502-84-5Relevant articles and documents
A sustainable water-tolerant catalyst with enhanced Lewis acidity: Dual activation of Cp2TiCl2 via ligand and solvent
Yang, Mingming,Wang, Yanyan,Jian, Yajun,Leng, Deying,Zhang, Weiqiang,Zhang, Guofang,Sun, Huaming,Gao, Ziwei
, (2020/11/04)
A new strategy was developed to enhance the activity of titanocene dichloride for the synthesis of 2,4-disubstituted-3H-benzo[b]-[1,4]diazepine derivatives by using Cp2TiCl2 as a pre-catalyst. The titanocene was activated in situ in the catalytic system via the coordination with m-phthalic acid and alcohol solvent accompanied with the secession of a cyclopentadienyl ring, leading to the formation of an activated species, [CpTi(OEt)2(η1-C8H5O4)]. In particular, the novel developed half-titanocene catalyst exhibited more superior stability than representative half-titanocene complex, indicated by not only water compatibility for the employment of 30 % aqueous ethanol solution but also the recyclability that the products could be generated without apparent yield decrease after 5 runs. In general, we present a paradigm for sustainable molecular catalysis of titanocene.
3H-1,5-Benzodiazepines from ethynyl ketones and o-phenylenediamines
Ried,Teubner
, p. 741 - 744 (2007/10/04)
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