2016
DOI: 10.1016/j.jnt.2016.01.027
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On multiplicative functions with f(p+q+n0)=f(p)+f(q)+f(n0)

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Cited by 51 publications
(68 citation statements)
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“…(32) The Pd(OAc) 2 /PhI(OAc) 2 system was subsequently used for the alkoxylation of N-[2-(pyridin-2-yl)propan-2-yl]benzamides (33) (34) and 2-aryl-N-[2-(pyridin-2-yl)propan-2-yl]acetamides at 90°C in 1:1 mixtures of p-xylene and a primary or secondary alcohol. [48] Dialkoxylated products were obtained in moderate to high yields [Equation (35)] except in the cases of substrates bearing a meta substituent, which were monomethoxylated [Equation (36)]. Similar reaction conditions were recently used for the efficient monomethoxylation of N-(benzo[c][1,2,5]thiadiazol-4yl)benzamides [Equation (37)].…”
Section: Amide Coordinating Groups and Related Tethersmentioning
confidence: 99%
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“…(32) The Pd(OAc) 2 /PhI(OAc) 2 system was subsequently used for the alkoxylation of N-[2-(pyridin-2-yl)propan-2-yl]benzamides (33) (34) and 2-aryl-N-[2-(pyridin-2-yl)propan-2-yl]acetamides at 90°C in 1:1 mixtures of p-xylene and a primary or secondary alcohol. [48] Dialkoxylated products were obtained in moderate to high yields [Equation (35)] except in the cases of substrates bearing a meta substituent, which were monomethoxylated [Equation (36)]. Similar reaction conditions were recently used for the efficient monomethoxylation of N-(benzo[c][1,2,5]thiadiazol-4yl)benzamides [Equation (37)].…”
Section: Amide Coordinating Groups and Related Tethersmentioning
confidence: 99%
“…It also seems of interest to mention the para-methoxylation of N-(quinolin-8-yl)butyramide, which cannot involve C(sp 2 )-H activation through a palladium chelate [Equation (62)]. [48,64,65] Scheme 5. Reluctant substrates.…”
Section: Ineffective Groupsmentioning
confidence: 99%
“…[4,59,63] The enhancement in emission intensity upon addition of Hg 2+ is due to the interaction of the metal ion with the nitrogen donors in the calix-aza-crown moiety, which restricted the intramolecular reductive electron transfer (PeT) quenching process, as the nitrogen atoms of the azacrown moiety binds with the positively charged metal ion. [30,47,57,59,64,65] The ESI-MS of 1 upon addition of Hg 2+ (5 fold excess) in acetonitrile exhibited 1:1 complex formation, the observed m/z peaks at 1258.75 and 1299.86 correspond to [1 -2H + -Cl -+ Hg 2+ ] + (calcd. 1258.34) and [1 -2H + -Cl -+ Hg 2+ + CH 3 CN] + (calcd.…”
Section: Ion-binding Propertymentioning
confidence: 99%
“…Binding of Hg 2+ with soft donor atoms such as nitrogen leaving oxygen uncoordinated has been demonstrated with similar calixarene-based ionophore. [27,64,69] On the other hand, preferential binding of Cu 2+ with harder donor atoms, which includes oxygen atoms of the OH, C=O and ether moiety has also been demonstrated. [37] Therefore, the two metal ions are not in competition for the same site, once one metal ion is coordinated, it has blocked the entry of another metal ion.…”
Section: Mechanistic Aspects Of Dual Mode Selectivitymentioning
confidence: 99%
“…29,30 Among these three up-regulated miRNAs, miR-494-3p has been reported to suppress the progression and metastasis of prostate cancer. 31 Overexpressed miR-494-3p has been shown to inhibit the growth and paracrine function of mesenchymal stem cells by targeting of Cdk6, Ccnd1 and VEGF. 32 Furthermore, a mouse model has revealed that miR-494-3p is related to glioma proliferation and invasion.…”
Section: Lc3-i Lc3-iimentioning
confidence: 99%