474555-29-8Relevant articles and documents
Facile Synthesis of 2-Fluorobenzofurans: 5-endo-trig Cyclization of β,β-Difluoro-o-hydroxystyrenes
Morioka, Ryutaro,Fujita, Takeshi,Ichikawa, Junji
, (2020/10/22)
Efficient synthetic methods were established for obtaining 2-fluorobenzofurans involving various substituents. Upon being treated with 1,8-diazabicyclo[5.4.0]undec-7-ene under microwave irradiation, the α-unsubstituted β,β-difluoro-o-hydroxystyrenes under
Stereoselective ring-opening polymerization of a racemic lactide by using achiral salen- and homosalen-aluminum complexes
Nomura, Nobuyoshi,Ishii, Ryohei,Yamamoto, Yoshihiko,Kondo, Tadao
, p. 4433 - 4451 (2008/02/09)
Highly isotactic polylactide or poly(lactic acid) is synthesized in a ring-opening polymerization (ROP) of racemic lactide with achiral salen- and homosalen-aluminum complexes (salenH2 = N,N′-bis(salicylidene) ethylene-1,2-diamine; homosalenH2 = N,N′-bis(salicylidene) trimethylene-1,3-diamine). A systematic exploration of ligands demonstrates the importance of the steric influence of the Schiff base moiety on the degree of isotacticity and the backbone for high activity. The complexes prepared in situ are pure enough to apply to the polymerizations without purification. The crystal structures of the key complexes are elucidated by X-ray diffraction, which confirms that they are chiral. However. analysis of the 1H and 13C NMR spec tra unambiguously demonstrates that their conformations are so flexible that the chiral environment of the complexes cannot be maintained in solution at 25°C and that the complexes are achiral under the polymerization conditions. The flexibility of the back-bone in the propagation steps is also documented. Hence, the isotacticity of the polymer occurs due to a chain-end control mechanism. The highest reactivity in the present system is obtained with the homosalen ligand with 2.2-dimethyl substituents in the backbone (ArCH=NCH2CMe2CH2N=CHAr), whereas tBuMe2Si substituents at the 3-positions of the salicylidene moieties lead to the highest selectivity (Pmeso,= 0.98; T m = 210°C). The ratio of the rate constants in the ROPs of racemic lactide and L-lactide is found to correlate with the stereoselectivity in the present system. The complex can be utilized in bulk polymerization, which is the most attractive in industry, although with some loss of stereoselectivity at high temperature, and the afforded polymer shows a higher melting temperature (Pmeso = 0.92, Tm up to 189°C) than that of homochiral poly(L-lactide) (Tm = 162-180°C). The "livingness" of the bulk polymerization at 130°C is maintained even at a high conversion (97-98%) and for an extended polymerization time (1-2 h).
Substituted N-Salicylidene β-Amino Alcohols. Preparation and Use as Chiral Ligands in Enantioselective Sulfoxidation and Conjugate Addition
Skarzewski, Jacek,Ostrycharz, Elzbieta,Siedlecka, Renata,Zielinska-Blajet, Mariola,Pisarski, Bartlomiej
, p. 743 - 757 (2007/10/03)
A high-yielding synthesis of optically active 3,5-disubstituted N-salicylidene β-amino alcohols 6, versatile chiral ligands, is developed. The catalytic use of D or L-N-(3-phenyl-5-nitrosalicylidene)valinol (6j) in enantioselective sulfoxidation reactions (H2O2/VO(acac)2) gives up to 95 percent e.e. The asymmetric conjugate addition of thiophenol to 2-cyclohexen-1-one catalyzed by Ti(OPr-i)4 and 6 leads to maximum of 31 percent e.e.
