Related Products of 252978-89-5, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 252978-89-5, Name is tert-Butyl 4-(1H-indol-4-yl)piperazine-1-carboxylate,introducing its new discovery.
New diamine bis-phenol compounds of salan- (HOPh’CHNH(CH2)2NHCHPh’OH, Ph? = 2,4-(CMe2Ph)C6H2, H2L1) and salen-type (HOPh??CHN(CHPh)2NCHPh??OH, Ph?? = 2,4-tBuC6H2, H2L2 and HOPh??CHN(1,1?-2-binaphthyl)NCHPh??OH, Ph?? = 2,4-tBuC6H2, H2L3), as well as their oxido vanadium derivatives are described. VO(OiPr)3 was used as starting material for the preparation of [VO(OiPr)(L1)], 1, [VO(OiPr)(L2)], 3, and (mu-O){[VO(OiPr)(mu-O)(L3)VO]}2, 5. An intramolecular redox process involving the reduction of V(V) to V(IV) converts 3 into [VO(L2)], 4. The reactions of 1 and 5 with Me3SiCl give [VOCl(L1)], 2, and [VOCl(L3)], 6, respectively. All complexes were tested as catalysts for the sulfoxidation of thioanisole using H2O2 as oxidant. In general, the compounds display high activity and selectivity, although salan-type complexes (1 and 2) perform better. Comparison of complexes 5 and 6 shows that the monomeric species is more active and selective. Well-defined complexes, 5 and 6, display better catalytic performance than systems using 1:1.5 [VO(acac)2] and H2L3.
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Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles