67502-84-5Relevant academic research and scientific papers
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.
AZIRIDINYL KETONES AND THEIR HETERO ANALOGS 4. ACIDOLYSIS OF 1,1a-DIHYDROAZIRINOQUINOXALINES
Orlov, V. D.,Yaremenko, F. G.,Kolos, N. N.,Pivnenko, N. S.,Lavrushin, V. F.
, p. 424 - 428 (2007/10/02)
The isomerization of 1,2-diaryl-1,1a-dihydroazirinoquinozalines into 3-aryl-2-benzylquinoxalines under the action of acids is considered.The structure of the compounds synthetised have been confirmed by IR and PMR spectroscopy.It has been shown tha
