Category: 103-25-3

Recently I am researching about BONDS; ACTIVATION; AMINATION; FUNCTIONALIZATION, Saw an article supported by the NIHUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) – USA [R01 GM126832, R35 GM134929, 1S10 OD020022-1]; Ruth L. Kirschstein NRSA fellowshipUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) – USA [F32 GM129909]; NSFNational Science Foundation (NSF) [CHE-1048642]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Vasilopoulos, A; Golden, DL; Buss, JA; Stahl, SS. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate. Formula: C10H12O2

Site-selective transformation of benzylic C-H bonds into diverse functional groups is achieved via Cu-catalyzed C-H fluorination with N-fluorobenzenesulfonimide (NFSI), followed by substitution of the resulting fluoride with various nucleophiles. The benzyl fluorides generated in these reactions are reactive electrophiles in the presence of hydrogen-bond donors or Lewis acids, allowing them to be used without isolation in C-O, C-N, and C-C coupling reactions.

Formula: C10H12O2. About Methyl 3-phenylpropionate, If you have any questions, you can contact Vasilopoulos, A; Golden, DL; Buss, JA; Stahl, SS or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Application In Synthesis of Methyl 3-phenylpropionate. In 2020.0 EUR J ORG CHEM published article about WATER; ALKYNES; REDUCTION; HYDROTRIFLUOROMETHYLATION; DIBORATION; H2O in [Lin, Xiao; Wang, Yuhan; Hu, Yan; Zhu, Wanjiang; Dou, Xiaowei] China Pharmaceut Univ, Sch Sci, Dept Chem, Longmian Ave 639, Nanjing 211198, Peoples R China in 2020.0, Cited 49.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3.

A diboron-mediated rhodium-catalysed transfer hydrogenation system using water as the hydrogen donor is developed. In addition to a series of alkenes with good functional group tolerance, this rhodium-based catalytic system also effectively reduces aldehydes and ketones. A plausible mechanism involving the Rh-I-catalysed hydrogen generation and Rh-0-catalysed hydrogenation is proposed for the reaction.

Application In Synthesis of Methyl 3-phenylpropionate. About Methyl 3-phenylpropionate, If you have any questions, you can contact Lin, X; Wang, YH; Hu, Y; Zhu, WJ; Dou, XW or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Application In Synthesis of Methyl 3-phenylpropionate. Recently I am researching about CARBOXYLIC-ACIDS; REDUCTION; EFFICIENT; CARBONYL; HYDROSILYLATION; HYDROGENATION; HYDROBORATION; COMPLEXES; LIGAND; MILD, Saw an article supported by the SERB New DelhiDepartment of Science & Technology (India)Science Engineering Research Board (SERB), India [EMR/2016/002517]; Department of Atomic EnergyDepartment of Atomic Energy (DAE); NISER; CSIRCouncil of Scientific & Industrial Research (CSIR) – India. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Pattanaik, S; Chidambaram, G. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

Efficient and selective reduction of esters to aldehydes and alcohols is reported in which a simple cobalt pincer catalyst catalyses both transformations using diethylsilane as a reductant. Remarkably, the reaction selectivity is controlled by the stoichiometry of diethylsilane.

Application In Synthesis of Methyl 3-phenylpropionate. About Methyl 3-phenylpropionate, If you have any questions, you can contact Pattanaik, S; Chidambaram, G or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Computed Properties of C10H12O2. Iosub, AV; Moravcik, S; Wallentin, CJ; Bergman, J in [Iosub, Andrei, V; Moravcik, Stefan; Bergman, Joakim] AstraZeneca, BioPharmaceut R&D, Med Chem Res & Early Dev Cardiovasc, Renal & Metab, Gothenburg, Sweden; [Wallentin, Carl-Johan] Gothenburg Univ, Dept Chem & Mol Biol, Gothenburg, Sweden published Nickel-Catalyzed Selective Reduction of Carboxylic Acids to Aldehydes in 2019.0, Cited 66.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3.

The direct reduction of carboxylic acids to aldehydes is a fundamental transformation in organic synthesis. The combination of an air-stable Ni precatalyst, dimethyl dicarbonate as an activator, and silane reductant effects this reduction for a wide variety of substrates, including pharmaceutically relevant structures, in good yields and with no overreduction to alcohols. Moreover, this methodology is scalable, allows access to deuterated aldehydes, and is also compatible with one-pot utilization of the aldehyde products.

Computed Properties of C10H12O2. About Methyl 3-phenylpropionate, If you have any questions, you can contact Iosub, AV; Moravcik, S; Wallentin, CJ; Bergman, J or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Taking electrodecarboxylative etherification beyond Hofer-Moest using a radical C-O coupling strategy WOS:000607085800015 published article about DECARBOXYLATIVE ALLYLIC ETHERIFICATION; OXIDATIVE DECARBOXYLATION; CARBOXYLIC-ACIDS; ANODIC-OXIDATION; ELECTROCHEMICAL SYNTHESIS; ALIPHATIC-ACIDS; MALONIC-ACID; ARYL; COMPLEXES; ELECTROLYSIS in [Martinez, Angel Manu; Hayrapetyan, Davit; van Lingen, Tim; Dyga, Marco; Goossen, Lukas J.] Ruhr Univ Bochum, Fak Chem & Biochem, Univ Str 150, D-44801 Bochum, Germany in 2020.0, Cited 75.0. HPLC of Formula: C10H12O2. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

Established electrodecarboxylative etherification protocols are based on Hofer-Moest-type reaction pathways. An oxidative decarboxylation gives rise to radicals, which are further oxidised to carbocations. This is possible only for benzylic or otherwise stabilised substrates. Here, we report the electrodecarboxylative radical-radical coupling of lithium alkylcarboxylates with 1-hydroxybenzotriazole at platinum electrodes in methanol/pyridine to afford alkyl benzotriazole ethers. The substrate scope of this electrochemical radical coupling extends to primary and secondary alkylcarboxylates. The benzotriazole products easily undergo reductive cleavage to the alcohols. They can also serve as synthetic hubs to access a wide variety of functional groups. This reaction prototype demonstrates that electrodecarboxylative C-O bond formation can be taken beyond the intrinsic substrate limitations of Hofer-Moest mechanisms.

HPLC of Formula: C10H12O2. About Methyl 3-phenylpropionate, If you have any questions, you can contact Martinez, AM; Hayrapetyan, D; van Lingen, T; Dyga, M; Goossen, LJ or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

I found the field of Chemistry very interesting. Saw the article The merger of decatungstate and copper catalysis to enable aliphatic C(sp(3))-H trifluoromethylation published in 2020.0. Category: esters-buliding-blocks, Reprint Addresses MacMillan, DWC (corresponding author), Princeton Univ, Merck Ctr Catalysis, Princeton, NJ 08544 USA.. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

The introduction of a trifluoromethyl (CF3) group can dramatically improve a compound’s biological properties. Despite the well-established importance of trifluoromethylated compounds, general methods for the trifluoromethylation of alkyl C-H bonds remain elusive. Here we report the development of a dual-catalytic C(sp(3))-H trifluoromethylation through the merger of light-driven, decatungstate-catalysed hydrogen atom transfer and copper catalysis. This metallaphotoredox methodology enables the direct conversion of both strong aliphatic and benzylic C-H bonds into the corresponding C(sp(3))-CF3 products in a single step using a bench-stable, commercially available trifluoromethylation reagent. The reaction requires only a single equivalent of substrate and proceeds with excellent selectivity for positions distal to unprotected amines. To demonstrate the utility of this new methodology for late-stage functionalization, we have directly derivatized a broad range of approved drugs and natural products to generate valuable trifluoromethylated analogues. Preliminary mechanistic experiments reveal that a ‘Cu-CF3’ species is formed during this process and the critical C(sp(3))-CF3 bond-forming step involves the copper catalyst.

About Methyl 3-phenylpropionate, If you have any questions, you can contact Sarver, PJ; Bacauanu, V; Schultz, DM; DiRocco, DA; Lam, YH; Sherer, EC; MacMillan, DWC or concate me.. Category: esters-buliding-blocks

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

In 2020.0 BMC NEUROL published article about GELATINASE B GENE; CEREBROSPINAL-FLUID; SUSCEPTIBILITY; MATRIX-METALLOPROTEINASE-9; PROMOTER; ASSOCIATION; HERITABILITY; MS; EXPRESSION; BIOMARKERS in [Mohammadhosayni, Mina] Shahed Univ, Dept Immunol, Fac Med, Tehran, Iran; [Khosrojerdi, Arezou] Tarbiat Modares Univ, Dept Med Immunol, Fac Med Sci, Tehran, Iran; [Lorian, Keivan] Univ Tehran Med Sci, Sch Med, Dept Physiol, Tehran, Iran; [Aslani, Saeed] Univ Tehran Med Sci, Sch Med, Dept Immunol, Tehran, Iran; [Imani, Danyal] Univ Tehran Med Sci, Sch Publ Hlth, Dept Immunol, Tehran, Iran; [Razi, Bahman] Tarbiat Modares Univ, Sch Med, Dept Hematol & Blood Transfus, Tehran, Iran; [Babaie, Farhad] Urmia Univ Med Sci, Cellular & Mol Res Ctr, Orumiyeh, Iran; [Torkamandi, Shahram] Urmia Univ Med Sci, Dept Med Genet & Immunol, Fac Med, Orumiyeh, Iran in 2020.0, Cited 61.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3. Quality Control of Methyl 3-phenylpropionate

Background Several studies have reported the association between polymorphisms in Matrix metalloproteinases (MMPs) gene family and risk of Multiple sclerosis (MS). However, the results have been inconsistent and inconclusive. To resolve this issue, here we performed a systematic review and meta-analysis of the MMP-91562 C/T (rs3918242), MMP-3 (- 1612 5A/6A), and MMP-2 (- 1306 C/T) polymorphisms and susceptibility to MS. Methods We conducted a comprehensive systematic search in the major electronic database, including Scopus and PubMed to look up for relevant studies published before December 2019 that surveyed the association between the MMP-91562 C/T (rs3918242), MMP-3 (- 1612 5A/6A), and MMP-2 (- 1306 C/T) polymorphisms and susceptibility to MS. The level of association between the polymorphisms and susceptibility to MS in the polled analysis was determined by calculating the odds ratio (OR) and the corresponding 95% confidence interval (CI). Results We found 15 studies containing 2430 MS subjects and 2304 controls. A statistically significant association was observed in the all five comparisons of the MMP-91562 C/T polymorphism and MS risk as follows: dominant model (OR = 1.62, 95% CI = 1.03-2.53, P = 0.03), recessive model (OR = 2.69, 95% CI = 1.68-4.29, P < 0.001), allelic model (OR = 1.51, 95% CI = 1-2.28, P = 0.04), TT vs. CC model (OR = 3.20, 95% CI = 1.87-5.46, P < 0.001), and CT vs. CC model (OR = 1.53, 95% CI = 1.02-2.28, P = 0.04). Conclusions Our meta-analysis revealed significant association of MMP-9 (- 1562 C/T) Single-nucleotide polymorphism (SNP) with MS susceptibility that increased the disease risk. About Methyl 3-phenylpropionate, If you have any questions, you can contact Mohammadhosayni, M; Khosrojerdi, A; Lorian, K; Aslani, S; Imani, D; Razi, B; Babaie, F; Torkamandi, S or concate me.. Quality Control of Methyl 3-phenylpropionate

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

I found the field of Chemistry very interesting. Saw the article N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts published in 2020.0. HPLC of Formula: C10H12O2, Reprint Addresses Hong, S (corresponding author), Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea.; Hong, S (corresponding author), Inst for Basic Sci Korea, Ctr Catalyt Hydrocarbon Functionalizat, Daejeon 34141, South Korea.. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

By employing an N-heterocyclic carbene (NHC) catalyst, we developed a versatile catalytic system that enables deaminative cross-coupling reactions of aldehydes with redox-active pyridinium salts. Katritzky pyridinium salts behave as single-electron oxidants capable of generating alkyl radicals enabled by the redox properties of the enolate form of Breslow intermediates. The resultant alkyl radical undergoes efficient recombination with the NHC-bound aldehyde-derived carbonyl carbon radical for the formation of a C-C bond. The mild and transition metal-free reaction conditions tolerate a broad range of functional groups, and its utility has been further demonstrated by the modification of a series of peptide feedstocks and application to the three-component dicarbofunctionalization of olefins.

HPLC of Formula: C10H12O2. About Methyl 3-phenylpropionate, If you have any questions, you can contact Kim, I; Im, H; Lee, H; Hong, S or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Hydrosilane-Promoted Facile Deprotection of tert-Butyl Groups in Esters, Ethers, Carbonates, and Carbamates WOS:000459822800003 published article about SILANE-REDUCTION; HECK REACTIONS; PALLADIUM; CLEAVAGE; CLUSTER; POLYMERIZATION; ALDEHYDES; REMOVAL in [Ikeda, Takuya; Zhang, Zhenzhong; Motoyama, Yukihiro] Toyota Technol Inst, Dept Adv Sci & Technol, Nagoya, Aichi 4688511, Japan in 2019.0, Cited 22.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3. SDS of cas: 103-25-3

Combination of PdCl2 with 1,1,3,3-tetramethyldisiloxane in the presence of activated carbon was found to be an effective catalyst system for the cleavage reaction of C-O bond of O-t-Bu moieties. The present catalytic reaction offers a practical method for the deprotection of tert-butyl esters, tert-butyl ethers, O-Boc, and N-Boc derivatives under mild conditions. The addition of activated carbon in the reaction mixture was proved to be crucial for not only sustaining the catalytic activity but also trapping the palladium species after the reaction.

About Methyl 3-phenylpropionate, If you have any questions, you can contact Ikeda, T; Zhang, ZZ; Motoyama, Y or concate me.. SDS of cas: 103-25-3

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Fullerene Derivatives as Lung Cancer Cell Inhibitors: Investigation of Potential Descriptors Using QSAR Approaches WOS:000525324200001 published article about EPIDEMIOLOGY; MATURATION; DESIGN; VIRUS; ACID; C-60 in [Huang, Hung-Jin; Hsu, Shan-hui] Natl Taiwan Univ, Inst Polymer Sci & Engn, 1,Sec 4 Roosevelt Rd, Taipei 10617, Taiwan; [Huang, Hung-Jin; Hsu, Shan-hui] Natl Hlth Res Inst, Inst Cellular & Syst Med, Miaoli, Taiwan; [Kraevaya, Olga A.; Troshin, Pavel A.] Skolkovo Inst Sci & Technol, Moscow, Russia; [Kraevaya, Olga A.; Voronov, Ilya I.; Troshin, Pavel A.] Russian Acad Sci, Inst Problems Chem Phys, Chernogolovka 142432, Russia; [Hsu, Shan-hui] Natl Taiwan Univ, Res & Dev Ctr Med Devices, Taipei, Taiwan in 2020.0, Cited 43.0. HPLC of Formula: C10H12O2. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

Background: Nanotechnology-based strategies in the treatment of cancer have potential advantages because of the favorable delivery of nanoparticles into tumors through porous vasculature. Materials and Methods: In the current study, we synthesized a series of water-soluble fullerene derivatives and observed their anti-tumor effects on human lung carcinoma A549 cell lines. The quantitative structure-activity relationship (QSAR) modeling was employed to investigate the relationship between anticancer effects and descriptors relevant to peculiarities of molecular structures of fullerene derivatives. Results: In the QSAR regression model, the evaluation results revealed that the determination coefficient r(2) and leave-one-out cross-validation q(2) for the recommended QSAR model were 0.9966 and 0.9246, respectively, indicating the reliability of the results. The molecular modeling showed that the lack of chlorine atom and a lower number of aliphatic single bonds in saturated hydrocarbon chains may be positively correlated with the lung cancer cytotoxicity of fullerene derivatives. Synthesized water-soluble fullerene derivatives have potential functional groups to inhibit the proliferation of lung cancer cells. Conclusion: The guidelines obtained from the QSAR model might strongly facilitate the rational design of potential fullerene-based drug candidates for lung cancer therapy in the future.

HPLC of Formula: C10H12O2. About Methyl 3-phenylpropionate, If you have any questions, you can contact Huang, HJ; Kraevaya, OA; Voronov, II; Troshin, PA; Hsu, SH or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics