Day: April 13, 2022

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Terpyridine Zn(II), Ru(III), and Ir(III) Complexes: The Relevant Role of the Nature of the Metal Ion and of the Ancillary Ligands on the Second-Order Nonlinear Response of Terpyridines Carrying Electron Donor or Electron Acceptor Groups, published in 2005-11-28, which mentions a compound: 89972-77-0, mainly applied to transition metal terpyridine complex preparation NLO; terpyridine derivative preparation complexation transition metal hyperpolarizability; geometry optical aminphenylterpyridine, Related Products of 89972-77-0.

Coordination of 4′-(C6H4-p-X)-2,2′:6′,2”-terpyridines [X = NO2, NBu2, (E)-CH:CHC6H4-p-NBu2, (E,E)-(CH:CH)2C6H4-p-NMe2] to Zn(II), Ru(III), and Ir(III) metal centers induces a significant enhancement of the absolute value of the 2nd-order nonlinear optical (NLO) response of the terpyridine, measured by both elec. field induced 2nd harmonic generation and solvatochromic methods. By varying the nature of the metal center, the enhanced 2nd-order NLO response shifts from pos. to neg. Such a shift is controlled by electronic charge-transfer transitions, such as metal-to-ligand or ligand-to-metal transitions, in addition to the intraligand charge transfer. The enhancement generated by coordination is also controlled by the chelation effect and by fine-tuning of the ancillary ligands.

Although many compounds look similar to this compound(89972-77-0)Related Products of 89972-77-0, numerous studies have shown that this compound(SMILES:CC1=CC=C(C2=CC(C3=NC=CC=C3)=NC(C4=NC=CC=C4)=C2)C=C1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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: 494-52-0, is researched, SMILESS is C1(C=NC=CC=1)[C@@H]1CCCCN1, Molecular C10H14N2Journal, Article, Journal of Pharmaceutical and Biomedical Analysis called A simple dilute-and-shoot method for screening and simultaneous quantification of nicotine and alkaloid impurities in electronic cigarette refills (e-liquids) by UHPLC-DAD, Author is Barhdadi, Sophia; Desmedt, Bart; Courselle, Patricia; Rogiers, Vera; Vanhaecke, Tamara; Deconinck, Eric, the main research direction is nicotine alkaloid impurity quantification electronic cigarette liquid UHPLC DAD; Accuracy profiles; Impurities; Nicotine; UHPLC-DAD; e-cigarettes.Synthetic Route of C10H14N2.

The electronic cigarette (e-cigarette) has emerged as a popular alternative to the traditional hazardous tobacco cigarette. The substantial increase in e-cigarette use also urgently calls for controlling the quality of e-cigarette refill liquid products (e-liquids). Currently, the most important quality indicator of e-liquid products is the quantification of nicotine and its related impurities. Although different methods have been published to measure nicotine and impurity levels, the majority of them use a targeted LC-MS/MS approach. There is, however, a need for more robust quantification methods that are easy to implement in most control (industrial and governmental) laboratories Therefore, in this study, a simple dilute-and-shoot UHPLC-DAD method has been developed and validated for the simultaneous quantification of nicotine and its alkaloid impurities in electronic cigarette refills. An optimal separation of the alkaloids was achieved in a runtime of 11 min. The method was successfully validated using the “”total error”” approach in accordance with the validation requirements of ISO-17025. During this validation, interference between the target components and a number of popular flavouring compounds such as vanillin, maltol, ethylacetate, etc. could be excluded. In addition, small changes to the column temperature, pH and molar concentration of the mobile phase buffer were deliberately introduced to assess the robustness of the method. Only a slightly different outcome between the newly developed UV-detection method and the targeted MS approach was found, due to the sensitivity of the different detection techniques. However, in the context of quality control of nicotine related impurities, for which the European Pharmacopoeia limits are currently applied, the sensitivity of the UHPLC-DAD method was found to be within the acceptable range. Despite the somewhat lower selectivity of the newly developed UV-detection technique vs. a targeted LC-MS/MS approach, it may be concluded that this method is a suitable alternative for quality control purposes.

Although many compounds look similar to this compound(494-52-0)Synthetic Route of C10H14N2, numerous studies have shown that this compound(SMILES:C1(C=NC=CC=1)[C@@H]1CCCCN1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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

Quality Control of Basic copper carbonate. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Basic copper carbonate, is researched, Molecular CH2Cu2O5, CAS is 12069-69-1, about Catalytic Urea Synthesis from Ammonium Carbamate Using a Copper(II) Complex: A Combined Experimental and Theoretical Study. Author is Hanson, Danielle S.; Wang, Yigui; Zhou, Xinrui; Washburn, Erik; Ekmekci, Merve B.; Dennis, Donovan; Paripati, Amay; Xiao, Dequan; Zhou, Meng.

The synthesis of urea fertilizer is currently the largest CO2 conversion process by volume in the industry. In this process, ammonium carbamate is an intermediate en route to urea formation. We determined that the tetraammineaquacopper(II) sulfate complex, [Cu(NH3)4(OH2)]SO4, catalyzed the formation of urea from ammonium carbamate in an aqueous solution A urea yield of up to 18 ± 6% was obtained at 120°C after 15 h and in a high-pressure metal reactor. No significant urea formed without the catalyst. The urea product was characterized by Fourier transform IR (FT-IR), powder X-ray diffraction (PXRD), and quant. 1H{13C} NMR analyses. The [Cu(NH3)4(OH2)]SO4 catalyst was then recovered at the end of the reaction in a 29% recovery yield, as verified by FT-IR, PXRD, and quant. UV-vis spectroscopy. A precipitation method using CO2 was developed to recover and reuse 66 ± 3% of Cu(II). The catalysis mechanism was investigated by the d. functional theory at the B3LYP/6-31G** level with an SMD continuum solvent model. We determined that the [Cu(NH3)4]2+ complex is likely an effective catalyst structure. The study of the catalysis mechanism suggests that the coordinated carbamate with [Cu(NH3)4]2+ is likely the starting point of the catalyzed reaction, and carbamic acid can be involved as a transient intermediate that facilitates the removal of an OH group. Our work has paved the way for the rational design of catalysts for urea synthesis from the greenhouse gas CO2.

Although many compounds look similar to this compound(12069-69-1)Quality Control of Basic copper carbonate, numerous studies have shown that this compound(SMILES:O[Cu]OC(O[Cu]O)=O), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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: 3393-45-1, is researched, SMILESS is O=C1C=CCCO1, Molecular C5H6O2Journal, Article, Natural Products and Bioprospecting called Chemical Constituents from the Whole Plant of Cuscuta reflexa, Author is Aung, Tin Thu Thu; Xia, Meng-Yuan; Hein, Pyae Phyo; Tang, Rong; Zhang, Dong-Dong; Yang, Jun; Yang, Xue-Fei; Hu, Dong-Bao; Wang, Yue-Hu, the main research direction is chem constituent plant cuscuta reflexa; 2H-pyran-2-one glucosides; Cuscuta reflexa; Platelet aggregation; Porcine pancreatic lipase; Steroidal glucosides.Formula: C5H6O2.

Two new 2H-pyran-2-one glucosides, cuscutarosides A (1) and B (2), and one new steroidal glucoside, 7β-methoxy-β-sitosterol 3-O-β-glucopyranoside (3), together with 12 known compounds (4-15) were isolated from the whole plant of Cuscuta reflexa (Convolvulaceae) collected from Myanmar. The chem. structures of these new compounds were elucidated based on extensive spectroscopic anal. The antiobesity activity of these isolates was evaluated using porcine pancreatic lipase (PPL), and the antiplatelet aggregation activity was screened using rabbit platelets induced by thrombin, platelet-activating factor (PAF), arachidonate (AA), or collagen. 7β-Methoxy-β-sitosterol 3-O-β-glucopyranoside (3) showed weak PPL inhibitory activity. Cuscutaroside A (1), its acetylated derivative (1a), and scrophenoside B (8) showed weak inhibitory activity against rabbit platelet aggregation induced by collagen. Compound 1a also showed inhibitory activity against rabbit platelet aggregation induced by AA.

Compounds in my other articles are similar to this one(5,6-Dihydro-2H-pyran-2-one)Formula: C5H6O2, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

Formula: C10H14N2. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: (S)-3-(Piperidin-2-yl)pyridine, is researched, Molecular C10H14N2, CAS is 494-52-0, about Ethylene response factor NtERF91 positively regulates alkaloid accumulations in tobacco (Nicotiana tabacum L.).

Tobacco alkaloid metabolism is regulated by various transcription factors (TFs). Here, we have characterized a non-NIC2 locus gene, Ethylene Response Factor 91 (ERF91), function in regulation of alkaloid accumulation in tobacco. NtERF91 was preferentially expressed in roots and induced by jasmonic acid. Addnl., NtERF91 was able to in vitro bind to the NtPMT2 and NtQPT2 promoters via directly targeting the GCC-box elements and transactivate NtQPT2 gene expression. Ectopic overexpression of NtERF91 not only increased the expression of most nicotine biosynthetic genes, but also altered alkaloid accumulation profile, resulting in dramatically anatabine accumulation. We conclude that NtERF91 plays an overlapped but distinct role in regulating tobacco alkaloid accumulations.

Compounds in my other articles are similar to this one((S)-3-(Piperidin-2-yl)pyridine)Formula: C10H14N2, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Synthesis of the chiral synthon for the enantioselective syntheses of the eburnamine type alkaloids, published in 1982-08-01, which mentions a compound: 32780-06-6, mainly applied to eburnamine synthon chiral enantioselective, Synthetic Route of C5H8O3.

A chiral synthon (I) for the syntheses of (-)-eburnamonine (II) and related eburnamine type alkaloids has been prepared in a good yield from the known compound (III) originated from L-glutamic acid or D-mannitol.

Compounds in my other articles are similar to this one((S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one)Synthetic Route of C5H8O3, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Tetrahedron Letters called Enantioselective synthesis of (-)-velbanamine and (+)-isovelbanamine using L-glutamic acid as chiral template, Author is Takano, Seiichi; Yonaga, Masahiro; Chiba, Kenji; Ogasawara, Kunio, which mentions a compound: 32780-06-6, SMILESS is O=C1O[C@H](CO)CC1, Molecular C5H8O3, Computed Properties of C5H8O3.

(-)-Velbanamine and (+)-isovelbanamine (I; R = Et, R1 = OH; R = OH, R1 = Et, resp.) were stereoselectively prepared from L-glutamic acid in 14 steps. I are potential intermediates for the Pandaca alkaloids in the natural configuration.

Compounds in my other articles are similar to this one((S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one)Computed Properties of C5H8O3, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

Reference of (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one, is researched, Molecular C5H8O3, CAS is 32780-06-6, about A synthetic approach to the pseudopterosins using cascade technology. Author is Harrowven, David C.; Dennison, Shelagh T.; Howes, Peter.

A rapid synthetic entry toward the pseudopterosins, a class of diterpenes which display potent antiinflammatory and analgesic properties, is described. The key feature of this approach is the use of a sequential intramol., Lewis acid mediated Friedel-Crafts alkylation-Friedel-Crafts acylation sequence, viz, lactone I to phenalenone II, to establish the tricyclic carbon framework.

Compounds in my other articles are similar to this one((S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one)Reference of (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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, Article, Journal of the American Chemical Society called Stereochemical Elucidation of Streptorubin B, Author is Haynes, Stuart W.; Sydor, Paulina K.; Corre, Christophe; Song, Lijiang; Challis, Gregory L., the main research direction is stereochem streptorubin B Streptomyces enantioselective synthesis.Formula: C5H8O3.

Streptorubin B is a structurally remarkable member of the prodiginine group of antibiotics produced by several actinobacteria, including the model organism Streptomyces coelicolor A3. Transannular strain within the pyrrolophane structure of this mol. causes restricted rotation that gives rise to the possibility of (diastereomeric) atropisomers. Neither the relative nor the absolute stereochem. of streptorubin B is known. NOESY NMR experiments were used to define the relative stereochem. of the major atropisomer of streptorubin B·HCl in solution as anti. We exploited this finding together with our knowledge of streptorubin B biosynthesis in S. coelicolor to determine the absolute stereochem. of the anti atropisomer. 2-Undecylpyrrole stereoselectively labeled with deuterium at C-4′ was synthesized and fed to a mutant of S. coelicolor, which was unable to produce streptorubin B because it was blocked in 2-undecylpyrrole biosynthesis, and in which the genes responsible for the last two steps of streptorubin B biosynthesis were overexpressed. 1H and 2H NMR anal. of the stereoselectively deuterium-labeled streptorubin B·HCl produced by this mutasynthesis strategy allowed us to assign the absolute stereochem. of the major (anti) atropisomer as 7’S. HPLC analyses of streptorubin B isolated from S. coelicolor on a homochiral stationary phase and comparisons with streptorubin B derived from an enantioselective synthesis showed that the natural product consists of an approx. 88:7:5 mixture of the (7’S, anti), (7’S, syn), and (7’R, anti) stereoisomers.

Compounds in my other articles are similar to this one((S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one)Formula: C5H8O3, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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: (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one(SMILESS: O=C1O[C@H](CO)CC1,cas:32780-06-6) is researched.HPLC of Formula: 123333-71-1. The article 《Design and SAR study of a novel class of nucleotide analogues as potent anti-HCMV agents》 in relation to this compound, is published in Nucleosides & Nucleotides. Let’s take a look at the latest research on this compound (cas:32780-06-6).

We have developed a novel class of 2-phosphonate 1,3-dioxolane nucleotide analogs, from which the guanine derivative displayed weak anti-HCMV activity. Further SAR studies led to the identification of both cis and trans guanine derivatives of THF analogs as potent anti-HCMV agents, both in vitro and in vivo, compared to ganciclovir and HPMPC.

Compounds in my other articles are similar to this one((S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one)Reference of (S)-5-(Hydroxymethyl)dihydrofuran-2(3H)-one, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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