Category: catalyst-ligand

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 6-(Piperazin-1-yl)nicotinonitrile, is researched, Molecular C10H12N4, CAS is 149554-29-0, about The discovery of potent antagonists of NPBWR1 (GPR7).Application In Synthesis of 6-(Piperazin-1-yl)nicotinonitrile.

The synthesis and evaluation of small mol. antagonists of the G protein-coupled receptor NPBWR1 (GPR7) are reported for the first time. [4-(5-Chloropyridin-2-yl)piperazin-1-yl][(1S,2S,4R)-4-{[(1R)-1-(4-methoxyphenyl)ethyl]amino}-2-(thiophen-3-yl)cyclohexyl]methanone (I) emerged as a hit from a high-throughput screen. Examination of substituents that focused on replacing the 5-chloropyridine and 4-methoxybenzylamino groups of I led to the identification of compounds that exhibited subnanomolar potencies as low as 660 pM {II [X = NH]} in the functional assay and 200 pM in the binding assay {II [X = O]}.

In some applications, this compound(149554-29-0)Application In Synthesis of 6-(Piperazin-1-yl)nicotinonitrile is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one, is researched, Molecular C5H8O3, CAS is 32780-06-6, about Plant growth regulators and Axl and immune checkpoint inhibitors from the edible mushroom Leucopaxillus giganteus, the main research direction is Leucopaxillus lung cancer anticancer plant growth regulator Axl PDL1; Leucopaxillus giganteus ; Axl inhibitor; immune checkpoint inhibitor; plant growth regulator; structure determination.Formula: C5H8O3.

A novel compound, (R)-4-ethoxy-2-hydroxy-4-oxobutanoic acid (), and six known compounds (-) were isolated from the fruiting bodies of the wild edible mushroom Leucopaxillus giganteus. The planar structure of was determined by the interpretation of spectroscopic data anal. The absolute configuration of was determined by comparing sp. rotation of the synthetic compounds In the plant regulatory assay, the isolated compounds (-) and the chem. prepared compounds (-) were evaluated their biol. activity against the lettuce (Lactuca sativa) growth. Compounds and – showed the significant regulatory activity of lettuce growth. showed the strongest inhibition activity among the all the compounds tested. In the lung cancer assay, all the compounds were assessed the mRNA expression of Axl and immune checkpoints (PD-L1, PD-L2) in the human A549 alveolar epithelial cell line by RT-PCR. Compounds – showed significant inhibition activity against Axl and/or immune checkpoint.

In some applications, this compound(32780-06-6)Formula: C5H8O3 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 89972-77-0, is researched, SMILESS is CC1=CC=C(C2=CC(C3=NC=CC=C3)=NC(C4=NC=CC=C4)=C2)C=C1, Molecular C22H17N3Journal, Article, Angewandte Chemie, International Edition called Self- and directed assembly of hexaruthenium macrocycles, Author is Newkome, George R.; Cho, Tae Joon; Moorefield, Charles N.; Baker, Gregory R.; Cush, Randy; Russo, Paul S., the main research direction is ruthenium benzenebisterpyridine complex macrocycle self assembly preparation; terpyridine benzenebis ruthenium complex macrocycle self assembly.SDS of cas: 89972-77-0.

The bis(terpyridyl) ligands 5-bromo- and 5-methyl-benzene-1,3-diylbis-4′-(2,2′:6′,2”-terpyridine) were prepared and complexed with ruthenium to give mono- and dinuclear complexes which were self-assembled into hexaruthenium macrocycles. The ligands, complexes and macrocycles were characterized by elemental analyses and 1H NMR, UV and mass spectroscopy.

In some applications, this compound(89972-77-0)SDS of cas: 89972-77-0 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Quality Control of 4-(p-Tolyl)-2,2:6,2-terpyridine. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 4-(p-Tolyl)-2,2:6,2-terpyridine, is researched, Molecular C22H17N3, CAS is 89972-77-0, about Synthesis and co-crystallization behavior of copper(II) complexes of two isomeric p-tolyl-terpyridines. Author is Bray, David J.; Clegg, Jack K.; Jolliffe, Katrina A.; Lindoy, Leonard F.; Wei, Gang.

Cu(II) complexes incorporating the isomeric tolyl-derivatized terpyridine ligands, 4′-p-tolyl-2,2′:6′,2”-terpyridine (L1) and 6′-p-tolyl-2,2′:2”,4′-terpyridine (L2) were prepared and characterized by x-ray diffraction. The 1st of these is a co-crystal [Cu(L1)(NO3)2]·[Cu(L1)(NO3)(EtOH)]NO3·MeOH while the 2nd is a single complex [Cu(L2)2(NO3)]NO3·0.5MeOH·1.5H2O. Crystallization of a mixture of both products from EtOH/MeOH (1:1) yields an unusual co-crystalline product [Cu(L2)2NO3]2[Cu(L1)(NO3)2](NO3)2 whose structure was also confirmed by an x-ray structure determination

In some applications, this compound(89972-77-0)Quality Control of 4-(p-Tolyl)-2,2:6,2-terpyridine is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Lawler, Tameka S.; Stanfill, Stephen B.; Tran, Hang T.; Lee, Grace E.; Chen, Patrick X.; Kimbrell, J. Brett; Lisko, Joseph G.; Fernandez, Carolina; Caudill, Samuel P.; Rey de Castro, B.; Watson, Clifford H. published the article 《Chemical analysis of snus products from the United States and northern Europe》. Keywords: snus moisture nicotine TSNA United States Europe.They researched the compound: (S)-3-(Piperidin-2-yl)pyridine( cas:494-52-0 ).Safety of (S)-3-(Piperidin-2-yl)pyridine. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:494-52-0) here.

Snus is an oral tobacco product that originated in Sweden. Snus products are available as fine-cut loose tobacco or in pre-portioned porous “”pouches.”” Some snus products undergo tobacco pasteurization during manufacturing, a process that removes or reduces nitrite-forming microbes, resulting in less tobacco-specific nitrosamine content in the product. Some tobacco companies and researchers have suggested that snus is potentially less harmful than traditional tobacco and thus a potential smoking cessation aid or an alternative to continued cigarette consumption. Although snus is available in various countries, limited information exists on snus variants from different manufacturers. Moisture, pH, nicotine, and tobacco-specific N’-nitrosamines (TSNAs) were quantified in 64 snus products made by 10 manufacturers in the United States and Northern Europe (NE). Reported means, standard Errors, and differences are least-square (LS) estimates from bootstrapped mixed effects models, which accounted for correlation among repeated measurements. Minor alkaloids and select flavors were also measured. Among all product types, moisture (27.4%-59.5%), pH (pH 5.87-9.10), total nicotine (6.81-20.6 mg/g, wet), unprotonated nicotine (0.083-15.7 mg/g), and total TSNAs (390-4,910 ng/g) varied widely. The LS-mean unprotonated nicotine concentration of NE portion (7.72 mg/g, SE = 0.963) and NE loose (5.06 mg/g, SE = 1.26) snus were each significantly higher than US portion snus (1.00 mg/g, SE = 1.56). Concentrations of minor alkaloids varied most among products with the highest total nicotine levels. The LS-mean NNN+NNK were higher in snus sold in the US (1360 ng/g, SE = 207) than in NE (836 ng/g, SE = 132) countries. The most abundant flavor compounds detected were pulegone, eucalyptol, and menthol. Phys. and chem. characteristics of US and NE products labeled as snus can vary considerably and should not be considered “”equivalent””. Our findings could inform public health and policy decisions pertaining to snus exposure and potential adverse health effects associated with snus.

In some applications, this compound(494-52-0)Safety of (S)-3-(Piperidin-2-yl)pyridine is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 11-Bromoundecanoic acid(SMILESS: O=C(O)CCCCCCCCCCBr,cas:2834-05-1) is researched.SDS of cas: 616-14-8. The article 《Selectivity control in thiol-yne click reactions via visible light induced associative electron upconversion》 in relation to this compound, is published in Chemical Science. Let’s take a look at the latest research on this compound (cas:2834-05-1).

An associative electron upconversion was proposed as a key step determiningthe selectivity of thiol-yne coupling. The developed synthetic approach provided an efficient tool to access a comprehensive range of products-four types of vinyl sulfides were prepared in high yields and selectivity. Practically important transition-metal-free regioselective thiol-yne additionand formation of the demanding Markovnikov-type product by a radical photoredox process. The photochem. process was directly monitored by mass-spectrometry in a specially designed ESI-MS device with green laser excitation in the spray chamber. The proposed reaction mechanism was supported by experiments and DFT calculations

In some applications, this compound(2834-05-1)Application In Synthesis of 11-Bromoundecanoic acid is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 4-(p-Tolyl)-2,2:6,2-terpyridine, is researched, Molecular C22H17N3, CAS is 89972-77-0, about Effect of substituent of terpyridines on the DNA-interaction of polypyridyl ruthenium(II) complexes.COA of Formula: C22H17N3.

An octahedral complexes of ruthenium with 2,9-dimethyl-1,10-phenanthroline (dmphen) and substituted terpyridine were synthesized. The RuII complexes were characterized by elemental analyses, thermogravimetric analyses, magnetic moment measurements, FTIR, electronic, 1H NMR and FAB mass spectra. The binding strength and mode of interaction of the complexes with Herring Sperm DNA was studied using absorption titration and viscosity measurement studies. Results suggest that the substituent on terpyridine ligand affects the binding mode and binding ability of the complexes. Effect of time and ionic strength on DNA cleavage ability of complex also was studied by gel electrophoresis. Results suggest that >200 mM concentration of NaCl decreases the cleavage ability of complex.

In some applications, this compound(89972-77-0)COA of Formula: C22H17N3 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 32780-06-6, is researched, SMILESS is O=C1O[C@H](CO)CC1, Molecular C5H8O3Journal, Green Chemistry called Chemo-enzymatic synthesis of key intermediates (S)-γ-hydroxymethyl-α,β-butenolide and (S)-γ-hydroxymethyl-γ-butyrolactone via lipase-mediated Baeyer-Villiger oxidation of levoglucosenone, Author is Flourat, A. L.; Peru, A. A. M.; Teixeira, A. R. S.; Brunissen, F.; Allais, F., the main research direction is lipase Baeyer Villiger oxidation levoglucosenone.Reference of (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one.

Levoglucosenone (LGO), a valuable chiral platform chem. that can be efficiently produced from catalytic fast pyrolysis of cellulose, has been efficiently converted into optically pure (S)-γ-hydroxymethyl-α,β-butenolide (HBO) using a two-step sequence involving a lipase-mediated Baeyer-Villiger oxidation and an acid hydrolysis. In the same fashion, (S)-γ-hydroxymethyl-γ-butyrolactone (2H-HBO) was successfully obtained through a three-step sequence (Baeyer-Villiger, palladium-catalyzed hydrogenation and acid hydrolysis). The use of solid buffers in the lipase-mediated Baeyer-Villiger oxidation has proved beneficial in two ways: not only the reaction time and the enzymic load were both reduced four-fold (from 8 to 2 h and 464 to 113 U mmol-1) to reach conversions ≥83%, but solid buffers also prevented lipase from denaturation, thus preserving its enzymic activity and allowing its use for further oxidation cycles.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Computed Properties of C11H21BrO2. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 11-Bromoundecanoic acid, is researched, Molecular C11H21BrO2, CAS is 2834-05-1, about Design, synthesis, and biological evaluation of Bcr-Abl PROTACs to overcome T315I mutation. Author is Jiang, Liang; Wang, Yuting; Li, Qian; Tu, Zhengchao; Zhu, Sihua; Tu, Sanfang; Zhang, Zhang; Ding, Ke; Lu, Xiaoyun.

Bcr-Abl threonine 315 to isoleucine 315 (T315I) gatekeeper mutation induced drug resistance remains an unmet clin. challenge for the treatment of chronic myeloid leukemia (CML). Chem. degradation of Bcr-AblT315I protein has become a potential strategy to overcome drug resistance. Herein, we first described the design, synthesis, and evaluation of a new class of selective Bcr-AblT315I proteolysis-targeting chimeric (PROTAC) degraders based on GZD824 (reported as Bcr-AblT315I inhibitor by our group). One of the degrader 7o with 6-member carbon chain linkage with pomalidomide exhibits the most potent degradation efficacy with DR of 69.89% and 94.23% at 100 and 300 nmol/L, resp., and has an IC50 value of 26.8 ± 9.7 nmol/L against Ba/F3T315I cells. Further, 7o also displays substantial tumor regression against Ba/F3-Bcr-AblT315I xenograft model in vivo.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Pan, Qijun; Liu, Yongan; Pang, Wan; Wu, Jingjing; Ma, Xiaoyu; Hu, Xiaojun; Guo, Yong; Chen, Qing-Yun; Liu, Chao published an article about the compound: Basic copper carbonate( cas:12069-69-1,SMILESS:O[Cu]OC(O[Cu]O)=O ).Category: catalyst-ligand. 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:12069-69-1) through the article.

This paper reports a convenient copper-catalyzed three-component conversion of arylhydrazine hydrochlorides RNHNH2.HCl (R = 4-bromophenyl, naphthalen-2-yl, quinolin-7-yl, etc.) to arenesulfonyl fluorides RS(O)2F in good yields under mild conditions, using 1,4-diazabicyclo [2.2.2]octane bis(sulfur dioxide) (DABSO) as a sulfonyl source and N-fluorobenzenesulfonimide (NFSI) as a fluorine source based on a radical sulfur dioxide insertion and fluorination strategy. Notably, arylhydrazine hydrochloride is used as a safe precursor of aryl radicals.

In some applications, this compound(12069-69-1)Category: catalyst-ligand is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI