Hong, Sukwon; Tian, Shun; Metz, Matthew V.; Marks, Tobin J. published an article about the compound: Bis((S)-4-phenyl-4,5-dihydrooxazol-2-yl)methane( cas:132098-59-0,SMILESS:C1(CC2=N[C@@H](C3=CC=CC=C3)CO2)=N[C@@H](C4=CC=CC=C4)CO1 ).Electric Literature of C19H18N2O2. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:132098-59-0) through the article.
C2-sym. bis(oxazolinato)lanthanide complexes of the type [(4R,5S)-Ph2Box]La[N(TMS)2]2, [(4S,5R)-Ar2Box]La[N(TMS)2]2, and [(4S)-Ph-5,5-Me2Box]La[N(TMS)2]2 (Box = 2,2′-bis(2-oxazoline)methylenyl; Ar = 4-tert-butylphenyl, 1-naphthyl; TMS = SiMe3) serve as precatalysts for the efficient enantioselective intramol. hydroamination/cyclization of aminoalkenes and aminodienes. These new catalyst systems are conveniently generated in situ from the known metal precursors Ln[N(TMS)2]3 or Ln[CH(TMS)2]3 (Ln = La, Nd, Sm, Y, Lu) and 1.2 equiv of com. available or readily prepared bis(oxazoline) ligands such as (4R,5S)-Ph2BoxH, (4S,5R)-Ar2BoxH, and (4S)-Ph-5,5-Me2BoxH. The X-ray crystal structure of [(4S)-tBuBox]Lu[CH(TMS)2]2 provides insight into the structure of the in situ generated precatalyst species. Lanthanides having the largest ionic radii exhibit the highest turnover frequencies as well as enantioselectivities. Reaction rates maximize near 1:1 BoxH:Ln ratio (ligand acceleration); however, increasing the ratio to 2:1 BoxH:Ln decreases the reaction rate, while affording enantiomeric excesses similar to the 1:1 BoxH:Ln case. A screening study of bis(oxazoline) ligands reveals that aryl stereodirecting groups at the oxazoline ring 4 position and addnl. substitution (geminal di-Me or aryl) at the 5 position are crucial for high turnover frequencies and good enantioselectivities. The optimized precatalyst, in situ generated [(4R,5S)-Ph2Box]La[N(TMS)2]2, exhibits good rates and enantioselectivities, comparable to or greater than those achieved with chiral C1-sym. organolanthanocene catalysts, even for poorly responsive substrates (up to 67% ee at 23 °C). Kinetic studies reveal that hydroamination rates are zero order in [amine substrate] and first order in [catalyst], implicating the same general mechanism for organolanthanide-catalyzed hydroamination/cyclizations (intramol. turnover-limiting olefin insertion followed by the rapid protonolysis of an Ln-C bond by amine substrate) and implying that the active catalytic species is monomeric.
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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