28 research outputs found
Nickel-Catalyzed Phosphine Free Direct N‑Alkylation of Amides with Alcohols
Herein,
we developed an operational simple, practical, and selective
Ni-catalyzed synthesis of secondary amides. Application of renewable
alcohols, earth-abundant and nonprecious
nickel catalyst facilitates the transformations, releasing water as
byproduct. The catalytic system is tolerant to a variety of functional
groups including nitrile, allylic ether, and alkene and could be extended
to the synthesis of bis-amide, antiemetic drug Tigan, and dopamine
D2 receptor antagonist Itopride. Preliminary mechanistic studies revealed
the participation of a benzylic C–H bond in the rate-determining
step
Direct Synthesis of <i>Gem</i>-β,β′-Bis(alkyl) Alcohols Using Nickel Catalysis via Sequential DCR Approach
Chemoselective synthesis of functionalized gem-β,β′-bis(alkyl)alcohols
by coupling of a β-alkylated secondary alcohol with a primary
alcohol is reported using nickel via sequential DCR (dehydrogenation–condensation–rehydrogenation)
approach. Using our method, 1-arylethanol and benzyl alcohols undergo
a one-pot successive double alkylation reaction to form functionalized
alcohols. Methanol, C2–C12 alcohols, citronellol, and fatty
acid-derived oleic alcohols are tolerated, including late-stage functionalization
of steroid hormones (cholesterol and testosterone) and 5-pregnen-3β-ol-20-one.
The catalytic transformations enabled the synthesis of donepezil drug
(used for Alzheimer’s disease), N-heteroarenes
(quinoline and acridine), including chromane and intermediate flavan
derivatives. Hammett kinetic plot analysis of differently p-substituted benzyl alcohols with 1-phenyl propanol indicated
that the oxidation of benzyl alcohol might be the rate-determining
step and expected a strong influence of substitution on the reaction
kinetics. A negative ρ value (−0.60)
strongly signify the formation of the positive charge on benzyl alcohol.
Preliminary mechanistic investigation revealed that the dehydrogenation
of alcohol to aldehyde is the rate-determining step as it involves
the C–H/D bond breaking of the alcohol, and a PH/PD value of 6.0 was calculated.
Reaction profile studies, EPR experiments, Hammett-plot studies, cyclic
voltammetry, and UV–visible experiments, including XPS analysis,
indicated the structural and electronic changes at the Ni-center as
well as the behavior of the catalysts and alcohols during the progress
of the reactions
An Efficient and Selective Nickel-Catalyzed Direct N‑Alkylation of Anilines with Alcohols
Herein,
we developed an efficient and selective nickel-catalyzed
monoalkylation of various primary alcohols with aryl and heteroaryl
amines together with diols and amino alcohol derivatives. Notably,
the catalytic protocol consisting of an earth-abundant and non-precious
NiBr<sub>2</sub>/<b>L1</b> system enables the transformations
in the presence of hydroxyl, alkene, nitrile, and nitro functionalities.
As a highlight, we have demonstrated the alkylation of diamine, intramolecular
cyclization to N-heterocycles, and functionalization of complex vitamin
E, an (±)-α-tocopherol derivative. Preliminary mechanistic
studies revealed the participation of a benzylic C–H bond in
the rate-determining step
A concept "bank laws" in a wide and narrow value
Досліджено сутність поняття “банківське законодавство” в широкому і вузькому значенні.Essence of concept "bank laws" in a wide and narrow value is investigated
Palladium(II)-Catalyzed Tandem Oxidative Acetoxylation/<i>ortho</i> C–H Activation/Carbocyclization of Arylallenes
Herein
we report an example of tandem oxidative acetoxylation/carbocyclization
of arylallenes <b>1</b> using Pd(OAc)<sub>2</sub>. The catalytic
protocol is highly selective and provides access to new C–C
and C–O bonds leading to a carbocyclization. The reaction proceeds
via C–H activation by Pd. Mechanistic investigations show that
the C–H activation is not the rate-limiting step and indicate
that the reaction proceeds via acetoxylation of the allene
Increased Cytoplasmic Localization of p27<sup>kip1</sup> and Its Modulation of RhoA Activity during Progression of Chronic Myeloid Leukemia
<div><p>The role of p27<sup>kip1</sup> in Chronic Myeloid Leukemia (CML) has been well studied in relation to its function as a cell cycle inhibitor. However, its cytoplasmic function especially in CML remains to be seen. We studied the localization of p27<sup>kip1</sup> and its function during the progression of CML from chronic to blast phase. Our investigations revealed an increased localization of p27<sup>kip1</sup> in the cytoplasm of CD34<sup>+</sup> cells in the blast phase compared to chronic phase. Cytoplasmic p27<sup>kip1</sup> was found to modulate RhoA activity in CD34<sup>+</sup> stem and progenitor cells. Further, RhoA activity was shown to be dependent on cytoplasmic p27<sup>kip1</sup> which in turn was dependent on p210<sup>Bcr-Abl</sup> kinase activity. Interestingly, RhoA activity was observed to affect cell survival in the presence of imatinib through the SAPK/JNK pathway. Accordingly, inhibition of SAPK/JNK pathway using SP600125 increased apoptosis of K562 cells in presence of imatinib. Our results, for the first time, thus reveal a crucial link between cytoplasmic p27<sup>kip1</sup>, RhoA activity and SAPK/JNK signalling. To this effect we observed a correlation between increased cytoplasmic p27<sup>kip1</sup>, increased RhoA protein levels, decreased RhoA-GTP levels and increased SAPK/JNK phosphorylation in blast phase CD34<sup>+</sup> cells compared to chronic phase CD34<sup>+</sup> cells.</p> </div
RhoA activity affects cell survival.
<p>(A) K562 cells were transfected with MOCK, RhoAN19 or RhoAL63 vectors followed by treatment with 1µM imatinib for the indicated time points in hours. Cell lysates were assessed by western blot for the presence of pro-caspase3 and cleaved active caspase3. Beta actin was used as a loading control. Corresponding densitometric analysis indicates the mean±s.e.m of three independent experiments, (p<0.02). (B) K562 cells were transfected with MOCK, RhoAN19 or RhoAL63 vectors followed by treatment with/without 1µM imatinib. Cell survival was assessed by Annexin V staining. The plot shows the percent Annexin V positive staining population in three independent experiments (*p<0.005, **p<0.008) (C) K562 cells were transfected with GFP tagged MOCK, RhoAN19 or RhoAL63 vectors followed by treatment with/without 1µM imatinib for 24 hr. Cells were stained with anti cytochrome c antibody (red) and observed under the confocal microscope. The panel shows cytochrome c staining (red), GFP (green), differential interference contrast (DIC) image and a merged image of GFP and DIC. Release of cytochrome c from mitochondria gives a diffused cytochrome c staining as against the punctate staining pattern observed in cells with intact mitochondrial membrane permeability.</p
Inhibition of p210<sup>Bcr-Abl</sup> leads to increased JNK activity.
<p>(A) K562 cells were treated with imatinib with 1µM for 24 hr and the levels of phosphorylated p38 MAPK, p38MAPK, phosphorylated SAPK/JNK, SAPK/JNK phosphorylated p42/44 MAPK, p42/44 MAPK was assessed. Beta actin was used as a loading control. (B) K562 cells were transfected with MOCK, RhoAN19 or RhoAL63 vectors followed by treatment with/without 1µM imatinib for 24 hr. The levels of phosphorylated p38 MAPK, p38MAPK and phosphorylated SAPK/JNK, SAPK/JNK was assessed by western blotting. (C) K562 cells were treated with imatinib, C3 exozyme or both and the activity of SAPK/JNK pathway was assessed by looking into the phosphorylation of c-jun. (D) K562 cells were treated with imatinib, SP600125 or both and the level of cytochrome c released from the mitochondria was analysed in the mitochondria free cytosolic fraction. Tim23 was used to estimate mitochondrial contamination in the mitochondria free cytosolic preparations while beta actin was used as a loading control. (E) K562 cells were treated with the indicated concentrations of imatinib and SP600125 either singly or in combination for 24hrs. The percentage metabolic activity was assessed by MTT assay. Data shows the mean percent metabolic activity for individual treatments in three separate experiments. (F) K562 cells were treated with 1µM imatinib, 20µM SP600125 or both and apoptosis was measured by staining the cells with Annexin V and PI. Graph shows the change in Annexin V stained and Annexin V + PI stained population compared to untreated control cells (n=3, *p<0.037, **p<0.002). (G) Protein expression of phosphorylated SAPK/JNK, SAPK/JNK, phosphorylated c-jun and c-jun in CD34<sup>+</sup> cells of chronic and blast phase CML. Beta actin was used as a loading control.</p
Cytoplasmic p27<sup>kip1</sup> is dependent on p210<sup>Bcr-Abl</sup>.
<p>(A) K562 cells treated with the indicated doses (in µM) of imatinib for 24hrs were subjected to sub-cellular fractionation and the nuclear and cytoplasmic fractions were used to detect the levels of p27<sup>kip1</sup>. Lamin and GAPDH were used as loading controls for nuclear and cytoplasmic fractions respectively. Densitometric analysis indicates the mean ± s.e.m of three independent experiments with p<0.007 (B) K562 cells were treated with imatinib with the indicated dose (in µM) for 24 hr and the levels of phosphorylated p27 <sup>kip1</sup>S10 and p27<sup>kip1</sup> was assessed by western blotting. Beta actin was used as a loading control. (C) Primary chronic phase CML cells were treated with/without imatinib and then subjected to nuclear and cytoplasmic fractionation. The fractions were used to detect the levels of p27<sup>kip1</sup>. Histone 2B and GAPDH were used as loading controls for nuclear and cytoplasmic fractions respectively. The panel shows a densitometric analysis of three independent experiments with mean±s.e.m (p<0.01). (D) mRNA expression of p27<sup>kip1</sup> in chronic and blast phase CD34<sup>+</sup> stem and progenitor cells of CML was assessed by qRT-PCR. The expression was normalised against HPRT1. Horizontal bar indicates the mean of expression for the individual phase. (E) Protein expression of p27 <sup>kip1</sup>S10 and p27<sup>kip1</sup> in chronic and blast phase CD34<sup>+</sup> cells. Beta actin was used as a loading control. Densitometric analysis of the blots shows the mean ± s.e.m of 4 individual experiments (p<0.02). (F) Primary chronic and blast phase CML cells were subjected to nuclear and cytoplasmic fractionation. The fractions were used to detect the levels of p27<sup>kip1</sup>. Histone 2B and GAPDH were used as loading controls for nuclear and cytoplasmic fractions respectively. The panel shows a representative blot of two independent experiments. Densitometric analysis of two independent experiments has been shown with mean±s.e.m . Lower panel shows the fold change in expression of p27<sup>kip1</sup> in the cytoplasm of Blast phase CML cells compared to Chronic phase CML cells.</p
p210<sup>Bcr-Abl</sup> activity affects RhoA GTP levels.
<p>(A) Western blot showing the RhoA-GTP and total RhoA levels in K562 cells treated with/without imatinib. Corresponding densitometric analysis was performed after normalisation against beta actin (n=3, *p<0.004). (B) Western blot showing the RhoA-GTP and total RhoA levels in CML cells treated with/without imatinib. Corresponding densitometric analysis was performed after normalisation against beta actin (n=3, *p<0.0014). (C) CD34<sup>+</sup> stem and progenitor cells isolated from chronic phase CML bone marrow was nucleofected with the various constructs of p27<sup>kip1</sup>. The levels of RhoA-GTP and total RhoA were assessed in the resulting cells by western blotting. A representative blot of three independent experiments is shown (*p<0.09). (D) The distribution of RhoA between the membrane and cytosolic fraction under conditions of nucleotide exchange in K562 cells as observed by western blotting. (E) Ba/F3 cells were electroporated with p210 <sup>Bcr-Abl</sup>WT and p210 <sup>Bcr-Abl</sup>T315I and then treated with/ without imatinib. The western blot shows the expression of p210<sup>Bcr-Abl</sup> and Bcr proteins, the distribution of RhoA between the membrane and cytosolic fraction and corresponding levels of p27<sup>kip1</sup> and phosphorylated p27<sup>kip1</sup> S10 in these cells. Corresponding densitometric analysis shows the mean±s.e.m of three independent experiments (*p<0.09). (All the other plots have a p<0.002).</p