Category: 103-25-3

Recently I am researching about CHLOROFULLERENE C60CL6; DERIVATIVES; VIRUS; FUNCTIONALIZATION; INHIBITION; CHEMISTRY; BIOLOGY; C-60; 1ST, Saw an article supported by the Ministry for Science and Education [0089-2019-0010]; Russian Science FoundationRussian Science Foundation (RSF) [19-13-00411]. SDS of cas: 103-25-3. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Kraevaya, OA; Peregudov, AS; Troyanov, SI; Godovikov, I; Fedorova, NE; Klimova, RR; Sergeeva, VA; Kameneva, LV; Ershova, ES; Martynenko, VM; Claes, S; Kushch, AA; Kostyuk, SV; Schols, D; Shestakov, AF; Troshin, PA. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

We report an inversed Arbuzov reaction of the fullerene derivatives C60Ar5Cl with trialkyl phosphites P(OR)(3) producing alkylated fullerene derivatives C60Ar5R (R = Me, Et, iPr, nBu) with almost quantitative yields. This reaction provides a convenient synthetic route for the preparation of a large variety of functionalized fullerene derivatives with tailored properties, e.g. water-soluble compounds demonstrating promising antiviral activities against HCMV, HSV1, HIV and several influenza virus strains.

SDS of cas: 103-25-3. About Methyl 3-phenylpropionate, If you have any questions, you can contact Kraevaya, OA; Peregudov, AS; Troyanov, SI; Godovikov, I; Fedorova, NE; Klimova, RR; Sergeeva, VA; Kameneva, LV; Ershova, ES; Martynenko, VM; Claes, S; Kushch, AA; Kostyuk, SV; Schols, D; Shestakov, AF; Troshin, PA or concate me.

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

In 2020.0 INT J NANOMED 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. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3. HPLC of Formula: C10H12O2

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.

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.. HPLC of Formula: C10H12O2

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

Kim, I; Im, H; Lee, H; Hong, S in [Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea; [Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo] Inst for Basic Sci Korea, Ctr Catalyt Hydrocarbon Functionalizat, Daejeon 34141, South Korea published N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts in 2020.0, Cited 41.0. Formula: C10H12O2. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3.

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.

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

Application In Synthesis of Methyl 3-phenylpropionate. I found the field of Chemistry very interesting. Saw the article Catalytic asymmetric synthesis of 2,5-dihydrofurans using synergistic bifunctional Ag catalysis published in 2019.0, Reprint Addresses Chapman, E (corresponding author), Univ Arizona, Coll Pharm, Dept Pharmacol & Toxicol, Tucson, AZ 85721 USA.; Hu, WH (corresponding author), Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou, Guangdong, Peoples R China.. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate.

We report a bifunctional Ag catalyst promoted intramolecular capture of oxonium ylides with alkynes for the enantioselective synthesis of 2,5-dihydrofurans. This represents unprecedented synergistic catalysis of a bifunctional Ag catalyst. Mechanistic studies revealed that [(R)-3,5-DM-BINAP](AgSbF6)(2) (9) is likely to be the active catalytic species and that the reaction involves second order kinetics with respect to 9, suggesting that two molecules of 9 are involved in the intramolecular trapping of a Ag-associated oxonium ylide with a Ag-activated alkyne. Based on our mechanistic hypothesis, we further optimized the reaction, rendering a facile approach to 2,5-dihydrofurans in good to excellent yields in a highly chemo- and enantioselective fashion.

Application In Synthesis of Methyl 3-phenylpropionate. About Methyl 3-phenylpropionate, If you have any questions, you can contact Shi, TD; Teng, SH; Reddy, AGK; Guo, X; Zhang, YT; Moore, KT; Buckley, T; Mason, DJ; Wang, W; Chapman, E; Hu, WH or concate me.

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

Safety of Methyl 3-phenylpropionate. In 2019.0 ADV SYNTH CATAL 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.

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.

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

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

An article Synthesis and discovery of 18 beta-glycyrrhetinic acid derivatives inhibiting cancer stem cell properties in ovarian cancer cells WOS:000487054800018 published article about NATURAL-PRODUCTS; INVASION in [Li, Xiaojing; Wang, Na; Wang, Shuai; Wang, Hongmin] Liaocheng Univ, Sch Pharm, Lab Drug Discover & Design, Liaocheng 252000, Shandong, Peoples R China; [Li, Xiaojing] Shandong Univ, Sch Pharm, Minist Educ, Dept Med Chem,Key Lab Chem Biol, Jinan 250012, Shandong, Peoples R China; [Liu, Yihua; Ren, Shaoda] Liaocheng Peoples Hosp, Cent Lab, Liaocheng 252000, Shandong, Peoples R China; [Liu, Yuyu] Shandong Qidu Pharmaceut Co Ltd, Zibo 255400, Peoples R China; [Lie, Aihua] Liaocheng Peoples Hosp, Dept Obstet & Gynecol, Liaocheng 252000, Shandong, Peoples R China in 2019.0, Cited 23.0. Name: Methyl 3-phenylpropionate. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

Despite advances in ovarian cancer treatment, the five-year overall survival rate is less than 30% with the presence of cancer stem cells (CSCs). To develop CSC-targeting therapy, a series of 18 beta-glycyrrhetinic acid (GA) derivatives containing cinnamamide moiety have been designed, synthesized, and screened for their antiproliferative activity in SKOV3 and OVCAR3 cells. Most of the compounds exhibited stronger antiproliferative activity than GA, and compound 7c was the most active one. Further biological studies showed that compound 7c could induce apoptosis and suppress migration. In addition, compound 7c could not only observably decrease the colony formation and sphere formation ability, but also significantly reduce the CD44(+), CD133(+), and ALDH(+) subpopulation in SKOV3 and OVCAR3 cells. In conclusion, these results indicate that compound 7c is a promising anti-CSC agent for further anti-ovarian cancer studies.

Name: Methyl 3-phenylpropionate. About Methyl 3-phenylpropionate, If you have any questions, you can contact Li, XJ; Liu, YH; Wang, N; Liu, YY; Wang, S; Wang, HM; Lie, AH; Ren, SD or concate me.

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

Formula: C10H12O2. In 2020.0 ORG LETT published article about C-H SILYLATION; ELECTROPHILIC AROMATIC-SUBSTITUTION; BOND SILYLATION; PALLADIUM; ARYLATION; SALTS; FUNCTIONALIZATION; HETEROARENES; ACTIVATION in [Wang, Peng] Ctr Excellence Mol Synth, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China; [Wang, Peng] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Energy Regulat Mat, Shanghai 200032, Peoples R China; [Wu, Yichen; Huang, Yu-Hao; Chen, Xiao-Yue] Chinese Acad Sci, Shanghai Inst Organ Chem, Ctr Excellence Mol Synth, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China in 2020.0, Cited 68.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3.

The thianthrene S-oxide (TTSO)-mediated site-selective silylation of arenes has been realized via a thianthrenation/Pd-catalyzed silylation sequence. This method features a broad substrate scope and wide functional group tolerance under mild conditions and allows the synthesis of a set of (hetero)arylsilanes with operationally simple manipulations. The application and generality of the approach were further demonstrated by the late-stage functionalization of marketed drugs. This reaction also represents the first example of a Pd-catalyzed silylation reaction of aryl sulfonium salts.

About Methyl 3-phenylpropionate, If you have any questions, you can contact Wu, YC; Huang, YH; Chen, XY; Wang, P or concate me.. Formula: C10H12O2

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

Recommanded Product: 103-25-3. Recently I am researching about CHLOROFULLERENE C60CL6; DERIVATIVES; VIRUS; FUNCTIONALIZATION; INHIBITION; CHEMISTRY; BIOLOGY; C-60; 1ST, Saw an article supported by the Ministry for Science and Education [0089-2019-0010]; Russian Science FoundationRussian Science Foundation (RSF) [19-13-00411]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Kraevaya, OA; Peregudov, AS; Troyanov, SI; Godovikov, I; Fedorova, NE; Klimova, RR; Sergeeva, VA; Kameneva, LV; Ershova, ES; Martynenko, VM; Claes, S; Kushch, AA; Kostyuk, SV; Schols, D; Shestakov, AF; Troshin, PA. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

We report an inversed Arbuzov reaction of the fullerene derivatives C60Ar5Cl with trialkyl phosphites P(OR)(3) producing alkylated fullerene derivatives C60Ar5R (R = Me, Et, iPr, nBu) with almost quantitative yields. This reaction provides a convenient synthetic route for the preparation of a large variety of functionalized fullerene derivatives with tailored properties, e.g. water-soluble compounds demonstrating promising antiviral activities against HCMV, HSV1, HIV and several influenza virus strains.

About Methyl 3-phenylpropionate, If you have any questions, you can contact Kraevaya, OA; Peregudov, AS; Troyanov, SI; Godovikov, I; Fedorova, NE; Klimova, RR; Sergeeva, VA; Kameneva, LV; Ershova, ES; Martynenko, VM; Claes, S; Kushch, AA; Kostyuk, SV; Schols, D; Shestakov, AF; Troshin, PA or concate me.. Recommanded Product: 103-25-3

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

An article PCl3-mediated transesterification and aminolysis of tert-butyl esters via acid chloride formation WOS:000670481400019 published article about HIGHLY EFFICIENT; DIRECT AMIDATION; ESTERIFICATION; DERIVATIVES; OXIDATION; CATALYSIS; AMIDES; AMINES; GREEN; CONVERSION in [Wu, Xiaofang; Zhou, Lei; Li, Fangshao; Xiao, Jing] Hunan Univ Sci & Technol, Key Lab Theoret Organ Chem & Funct Mol, Minist Educ, Sch Chem & Chem Engn, Hunan Xiangtan Taoyuan Rd, Xiangtan 411201, Peoples R China in 2021.0, Cited 56.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3. Application In Synthesis of Methyl 3-phenylpropionate

A PCl3-mediated conversion of tert-butyl esters into esters and amides in one-pot under air is developed. This novel protocol is highlighted by the synthesis of skeletons of bioactive molecules and gram-scale reactions. Mechanistic studies revealed that this transformation involves the formation of an acid chloride in situ, which is followed by reactions with alcohols or amines to afford the desired products.

Application In Synthesis of Methyl 3-phenylpropionate. About Methyl 3-phenylpropionate, If you have any questions, you can contact Wu, XF; Zhou, L; Li, FS; Xiao, J or concate me.

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

In 2019.0 ADV SYNTH CATAL 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. Recommanded Product: 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.

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

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