نتایج جستجو برای: imine formation
تعداد نتایج: 529667 فیلتر نتایج به سال:
Planar chirality associated with the ferrocene in ferrocenyl oximes and hydrazones bearing chiral auxiliaries effectively competes with or overrides the normally excellent stereocontrol afforded by the auxiliary in determining the diastereoselectivity of addition to the C=N bond.
Molecular cages with arylboronate ester caps at the vertices are described. The were obtained by metal-templated polycondensation reactions of a tris(2-formylpyridine oxime) ligand arylboronic acids. Suited templates triflate or triflimide salts ZnII, FeII, CoII, MnII. In products, metal ions coordinated internally to pyridyl and oximato N atoms adjacent boronate ester, resulting in an improved...
A series of prototypical Co(II)-based pyridyl bis(imine) complexes {[2(ArN=C(Me))2C5H3N]CoCl2} (Ar = 2,6-C6H3Me2, 2,5-C6H3Me2, 2,4-C6H3Me2, 2,3C6H3Me2) bearing two methyl substituents on each imine aryl group are studied as precatalysts for the homopolymerization of 1,3-butadiene. They showed very high polymerization activities associated with ethylaluminum sesquichloride (EAS) as a cocatalyst....
The default explanation for good to high diastereomeric excess when reducing N-chiral imines possessing only mediocre cis/trans-imine ratios (>15% cis-imine) has invariably been in situ cis-to-trans isomerization before reduction; but until now no study unequivocally supported this conclusion. The present study co-examines an alternative hypothesis, namely that some classes of cis-imines may ho...
Pivalophenone N–H imine has been found to serve as a prominent substrate for directed C–H alkylation and arylation reactions with alkyl bromides and aryl chlorides, respectively, under cobalt–N-heterocyclic carbene (NHC) catalysis. Unlike the case of the parent pivalophenone imine, the increased steric bulk of the resulting ortho-substituted pivalophenone imines allows them to undergo clean imi...
Recent findings of a potential human carcinogen, acrylamide, in foods have focused research on the possible mechanisms of formation. We present a mechanism for the formation of acrylamide from the reaction of the amino acid asparagine and a carbonyl-containing compound at typical cooking temperatures. The mechanism involves formation of a Schiff base followed by decarboxylation and elimination ...
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