Month: October 2021

An article Three Resorcin[4]arene-Based Two-Dimensional Zn(II) Supramolecular Isomers Synthesized via a Structure-Directing Strategy for Knoevenagel Condensation WOS:000653539100055 published article about METAL-ORGANIC FRAMEWORKS; HETEROGENEOUS CATALYSTS; COORDINATION POLYMERS; AROMATIC-ALDEHYDES; MOLECULAR-SIEVE; SITES; MOFS; CONSTRUCTION; COMPLEXES; NETWORKS in [Wang, Fei-Fei; Liu, Ying-Ying; Pei, Wen-Yuan; Ma, Jian-Fang] Northeast Normal Univ, Dept Chem, Key Lab Polyoxometalate & Reticular Mat Chem, Changchun 130024, Peoples R China in 2021.0, Cited 51.0. Recommanded Product: 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Herein, in the presence of three structure-directing agents (SDAs), a family of imidazole-functionalized resorcin[4]arene-based coordination polymers (CPs), [Zn(TIC4R)(HCOO)]center dot HCOO center dot 0.5DMF center dot 1.5H(2)O (1), [Zn(TIC4R)(CN)]center dot HCOO center dot DMF center dot 2.5H(2)O (2), and [Zn(TIC4R)(H2O)]center dot 2HCOO center dot 2H(2)O (3), were assembled under solvothermal conditions [TIC4R = tetra(imidazole) resorcin[4]arene]. 1 exhibits a double-layer structure with rectangle windows, and 2 and 3 display monolayer structures. The layers of CPs 2 and 3 are slides with different offsets along the a-axis. In addition, three CPs were used as catalysts to catalyze Knoevenagel condensations. Strikingly, all CPs exhibit remarkable catalytic performance for several substrates. To the best of our knowledge, this is the first time that a small organic acid as SDA was used in the syntheses of resorcin[4]arene-based supra-molecular isomers.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Wang, FF; Liu, YY; Pei, WY; Ma, JF or concate me.. Recommanded Product: 4-Methoxybenzaldehyde

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In 2020 AICHE J published article about P-XYLENE OXIDATION; GAS-LIQUID; 2-PHASE FLOW; ACETIC-ACID; 2,5-FURANDICARBOXYLIC ACID; CATALYZED OXIDATION; TEREPHTHALIC ACID; PHASE OXIDATION; PRESSURE-DROP; AIR-OXIDATION in [Hommes, Arne; Disselhorst, Bas; Yue, Jun] Univ Groningen, Dept Chem Engn, Engn & Technol Inst Groningen, Nijenborgh 4, NL-9747 AG Groningen, Netherlands in 2020, Cited 57. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6. HPLC of Formula: C7H8O

Homogeneous Co/Mn/Br catalyzed aerobic oxidation of benzyl alcohol in acetic acid to benzaldehyde was performed in polytetrafluoroethylene microreactors operated under slug flow at temperatures up to 150 degrees C and pressures up to 5 bar. Depending on the bubble velocity and length, a wetted or dewetted slug flow was observed, characterized typically by a complete or partially wetting liquid film around the bubble body. The latter flow suffered from a limited interfacial area for mass transfer. Experiments at temperatures up to ca. 90 degrees C were under kinetic control given no product yield difference under wetted and dewetted slug flows and were used to establish a simplified kinetic expression (first order in benzyl alcohol and zero order in oxygen). This allows to develop a mass transfer model combined with an instantaneous reaction regime that well described the experimental results at higher temperatures where mass transfer was limiting in the dewetted slug flow.

HPLC of Formula: C7H8O. About Benzyl Alcohol, If you have any questions, you can contact Hommes, A; Disselhorst, B; Yue, J or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Category: indole-building-block. I found the field of Chemistry very interesting. Saw the article Cobalt(I)-Catalyzed Borylation of Unactivated Alkyl Bromides and Chlorides published in 2020, Reprint Addresses Geetharani, K (corresponding author), Indian Inst Sci, Dept Inorgan & Phys Chem, Bangalore 560012, Karnataka, India.. The CAS is 98-17-9. Through research, I have a further understanding and discovery of 3-(Trifluoromethyl)phenol.

A cobalt-complex-catalyzed borylation of a wide range of alkyl halides with a diboron reagent (B(2)pin(2) or B(2 )neop(2)) has been developed under mild reaction conditions, demonstrating the first cobalt-mediated cross-coupling with alkyl electrophiles. This protocol allows alkyl boronic esters to be accessed from alkyl halides, including alkyl chlorides, which were used rarely as coupling partners. Mechanistic studies reveal the possible involvement of an alkyl radical intermediate in this cobalt-mediated catalytic cycle.

Category: indole-building-block. About 3-(Trifluoromethyl)phenol, If you have any questions, you can contact Verma, PK; Prasad, KS; Varghese, D; Geetharani, K or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

COA of Formula: C7H6O2. In 2020.0 RSC ADV published article about CYSTEINE PROTEASE INHIBITORS; STABILITY in [Alves, Marina A.; Barreiro, Eliezer J.; Lima, Lidia M.] Univ Fed Rio De Janeiro UFRJ, Lab Avaliacao & Sintese Subst Bioativas LASSBio, Inst Nacl Ciencia & Tecnol Farmacos & Medicamento, CCS, POB 68023, BR-21941902 Rio De Janeiro, RJ, Brazil; [Alves, Marina A.; Barreiro, Eliezer J.; Lima, Lidia M.] Univ Fed Rio de Janeiro, Inst Quim, Programa Posgrad Quim, BR-21941909 Rio de Janeiro, RJ, Brazil; [de Queiroz, Aline C.; Leite, Anderson Brandao; Alexandre-Moreira, Magna S.] Univ Fed Alagoas UFAL, Inst Ciencias Biol & Sande, Lab Farmacol & Imunol, BR-57072900 Maceio, AL, Brazil; [Martins, Felipe T.; Doriguetto, Antonio C.] Univ Fed Goias, Inst Quim, Campus Samambaia,CP 131, BR-74001970 Goiania, Go, Brazil in 2020.0, Cited 33.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

Leishmaniasis is a neglected parasitic disease, and current treatment includes limitations of toxicity, variable efficacy, high costs and inconvenient doses and treatment schedules. Therefore, new leishmanicidal drugs are still an unquestionable medical need. In this paper we described the design conception of a new framework, the carbamoyl-N-aryl-imine-urea, to obtain putative leishmanicidal drug-candidates. Compounds 9a-e and 10a-e were designed and synthesized and their leishmanicidal activity was studied in comparison to pentamidine, miltefosine and meglumine antimoniate. The conformational profile of the new carbamoyl-N-aryl-imine-urea framework was investigated by X-ray diffraction studies, using compound 9a as a model. The plasma stability of this putative peptide mimetic subunit was studied for compound 10e (LASSBio-1736). Among the congeneric series, LASSBio-1736 was identified as a new antileishmanial drug-candidate, displaying plasma stability, cytotoxicity against amastigote forms of L. amazonensis and L. braziliensis, and leishmanicidal activity in a cutaneous leishmaniasis murine model, without preliminary evidence of hepatic or renal toxicity.

COA of Formula: C7H6O2. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Alves, MA; de Queiroz, AC; Leite, AB; Martins, FT; Doriguetto, AC; Barreiro, EJ; Alexandre-Moreira, MS; Lima, LM or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Catalyst-free visible-light induced synthesis of nitrogen- and oxygen-containing heterocycles from 1,3-diketones WOS:000604195100001 published article about ONE-POT SYNTHESIS; POLYHYDROQUINOLINE DERIVATIVES; ORGANIC-SYNTHESIS; CHEMISTRY in [Chen, Lu; Lin, Zhenyuan; Zhang, Xuefang; Tan, Leshi; Zhang, Min; Li, Yibiao] Wuyi Univ, Sch Biotechnol & Hlth Sci, Jiangmen, Peoples R China in 2021.0, Cited 40.0. Computed Properties of C9H10O3. The Name is 3,4-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 120-14-9

The synthesis of nitrogen- and oxygen-containing heterocycles has found many applications in the preparation of biomedical intermediates, yet actual synthetic procedures display limitations such as high-loading catalysts, harsh reaction conditions and tedious preparation of heterogeneous catalysts. Alternatively, photocatalysis allows to access functional products with minimum synthetic procedures and waste generation. Here, we present an efficient, simple, green protocol for the synthesis of N- and O-containing six-membered-ring compounds under mild conditions under visible blue light. Various aldehydes and 1,3-diketones can be reacted to afford eight series of corresponding 1,4-dihydropyridines and 4H-benzo[b]pyrans. This protocol has some merits such as the use of abundant and sustainable aqueous ethanol as solvent, short reaction time (within 60 min), no need of catalyst and broad functional group tolerance to afford 81 different series of target molecules in 75-96% yield under mild conditions.

Computed Properties of C9H10O3. About 3,4-Dimethoxybenzaldehyde, If you have any questions, you can contact Chen, L; Lin, ZY; Zhang, XF; Tan, LS; Zhang, M; Li, YB or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In 2020 ORG LETT published article about INSERTION in [Empel, Claire; Jana, Sripati; Pei, Chao; Koenigs, Rene M.] Rhein Westfal TH Aachen, Inst Organ Chem, D-52074 Aachen, Germany; [Empel, Claire; Thanh Vinh Nguyen; Koenigs, Rene M.] Univ New South Waley, Sch Chem, Sydney, NSW 2052, Australia in 2020, Cited 44. The Name is 3-(Trifluoromethyl)phenol. Through research, I have a further understanding and discovery of 98-17-9. Product Details of 98-17-9

In this work, we report a thorough investigation of the reaction of phenols with aryldiazoacetates. Mechanistic studies using different spectroscopic methods and theoretical calculations suggest a hydrogen bond between phenol and aryldiazoacetates, which can be modulated by the phenol acidity. The pK(A) of phenol and therefore the hydrogen bond plays an important role in a subsequent photoinduced proton transfer reaction to give the formal O-H functionalization product of phenols.

Product Details of 98-17-9. About 3-(Trifluoromethyl)phenol, If you have any questions, you can contact Empel, C; Jana, S; Pei, C; Nguyen, TV; Koenigs, RM or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In 2019.0 POLYMER published article about TRIDENTATE KETIMINATE LIGANDS; CYCLIC ESTERS; L-LACTIDE; EFFICIENT INITIATORS; CATALYTIC-ACTIVITY; METAL ALKOXIDES; IN-VITRO; COPOLYMERIZATION; SCAFFOLDS; DELIVERY in [Lai, Feng-Jie] Chi Mei Med Ctr, Dept Dermatol, Tainan, Taiwan; [Lai, Feng-Jie] Southern Taiwan Univ Sci & Technol, Ctr Gen Educ, Tainan, Taiwan; [Chiu, Li-Ling; Lee, Chieh-Ling; Lu, Wei-Yi; Lai, Yi-Chun; Ding, Shangwu; Chen, Hsuan-Ying] Kaohsiung Med Univ, Drug Dev & Value Creat Res Ctr, Dept Med & Appl Chem, Kaohsiung 80708, Taiwan; [Ding, Shangwu; Chen, Hsuan-Ying] Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan; [Chen, Hsuan-Ying] Kaohsiung Med Univ Hosp, Dept Med Res, Kaohsiung 80708, Taiwan; [Wu, Kuo-Hui] Univ Tokyo, Grad Sch Sci, Dept Chem, Tokyo 1130033, Japan in 2019.0, Cited 95.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6. COA of Formula: C7H8O

The ring-opening polymerizations of e-caprolactone (CL) using 5- and 6-membered ring Zn complexes bearing Schiff base as catalysts were comparatively studied. The 5-membered ring Zn complexes exhibited a considerably higher polymerization rate than the 6-membered ring Zn complexes (2-12 fold for CL polymerization) did. X-ray data revealed that 5-membered ring L-2(5-Ph) Zn creates larger empty space around the Zn center than 6-membered ring L-2(6-Bn) Zn. This allows higher interaction between the initiator and Zn complex and easy CL coordination.

COA of Formula: C7H8O. About Benzyl Alcohol, If you have any questions, you can contact Lai, FJ; Chiu, LL; Lee, CL; Lu, WY; Lai, YC; Ding, SW; Chen, HY; Wu, KH or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

I found the field of Chemistry very interesting. Saw the article 4-Hydroxy-3-methyl-2(1H)-quinolone, originally discovered from a Brassicaceae plant, produced by a soil bacterium of the genus Burkholderia sp.: determination of a preferred tautomer and antioxidant activity published in 2020. COA of Formula: C9H7NO2, Reprint Addresses Igarashi, Y (corresponding author), Toyama Prefectural Univ, Biotechnol Res Ctr, 5180 Kurokawa, Imizu, Toyama 9390398, Japan.; Igarashi, Y (corresponding author), Toyama Prefectural Univ, Dept Biotechnol, 5180 Kurokawa, Imizu, Toyama 9390398, Japan.. The CAS is 86-95-3. Through research, I have a further understanding and discovery of 4-Hydroxyquinolin-2(1H)-one

4-Hydroxy-3-methyl-2(1H)-quinolone (1), a molecule known for a long time and recently discovered from a Brassicaceae plant Isatis tinctoria without providing sufficient evidence to support the structure, was isolated from a fermentation extract of Burkholderia sp. 3Y-MMP isolated from a soil by a Zn2+ enrichment culture. Detailed spectroscopic analyses by MS and NMR, combined with C-13 chemical shift comparison with literature values of the related compounds and a synthetic preparation of 1, allowed its first full NMR characterization and identification of 2-quinolone but not 2-quinolinol (2) as the preferred tautomer for this heterocyclic system. While the metal-chelating activity was negligible, compound 1 at 10 mu M, a concentration lower than that in liquid production cultures, quenched hydroxy radical-induced chemiluminescence emitted by luminol by 86%. Because some Burkholderia species are pathogenic to plants and animals, the above result suggests that 1 is a potential antioxidant to counteract reactive oxygen species-based immune response in the host organisms.

COA of Formula: C9H7NO2. About 4-Hydroxyquinolin-2(1H)-one, If you have any questions, you can contact Li, DD; Oku, N; Shinozaki, Y; Kurokawa, Y; Igarashi, Y or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

HPLC of Formula: C8H8O2. Sultan, A; Shajahan, S; Ahamad, T; Alshehri, SM; Sajjad, N; Mehr-un-Nisa; Rehman, MHU; Torun, L; Khalid, M; Acevedo, R in [Sultan, Aeysha; Mehr-un-Nisa; Rehman, Mian Habib Ur] Univ Educ, Dept Chem, Faisalabad Campus, Faisalabad, Pakistan; [Shajahan, Shanavas] Periyar Univ, Dept Phys, Nano & Hybrid Mat Lab, Salem 636011, India; [Ahamad, Tansir; Alshehri, Saad M.] King Saud Univ, Coll Sci, Dept Chem, POB 2455, Riyadh 11451, Saudi Arabia; [Sajjad, Noreen] Univ Lahore, Dept Chem, Lahore, Pakistan; [Torun, Lokman] Yilditz Univ Engn & Technol, Dept Chem, Istanbul, Turkey; [Khalid, Muhammad] Khawaja Ghulam Fareed Univ Engn & Technol, Dept Chem, Rahim Yar Khan, Pakistan; [Acevedo, Roberto] Univ San Sebastian, Fac Ingn & Tecnol, Bellavista 7, Santiago 420524, Chile published Silica-supported heterogeneous catalysts-mediated synthesis of chalcones as potent urease inhibitors: in vitro and molecular docking studies in 2020.0, Cited 43.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

We herein report a facile and high yielding protocol for silica-supported heterogeneous catalysts-mediated synthesis of chalcones. A comparison of results of our synthesis with conventional synthetic protocols is also being offered to assess the efficiency of the prepared catalysts. Biological evaluation of the newly synthesized compounds as urease inhibitors was performed. Most of the compounds were found to have potent urease inhibition activity. The chalcone 3-(3-hydroxyphenyl)-1-phenylpropenone was found to be the most potent with percentage inhibition 86.17 +/- 0.89 and half maximal inhibitory concentration (IC50) value 11.51 +/- 0.03 mu M. The molecular docking study emphasized that the same congeners 3-(furan-2-yl)-1-(4-hydroxyphenyl)propenone, 3-(4-hydroxyphenyl)-1-(4-methoxyphenyl)propanone, and 3-[4-(dimethylamino)phenyl]-1-(p-tolyl)propenone showed very good inhibitory potential against urease and show a higher docking scores 5718, 5940, 5596 and an ACE of – 246.66, – 244.79, and – 243.06 kJ/mol, respectively than the control ligand.

HPLC of Formula: C8H8O2. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Sultan, A; Shajahan, S; Ahamad, T; Alshehri, SM; Sajjad, N; Mehr-un-Nisa; Rehman, MHU; Torun, L; Khalid, M; Acevedo, R or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article 4-Hydroxy-3-methyl-2(1H)-quinolone, originally discovered from a Brassicaceae plant, produced by a soil bacterium of the genus Burkholderia sp.: determination of a preferred tautomer and antioxidant activity WOS:000548343000001 published article about 2,4-DIHYDROXYQUINOLINE; DERIVATIVES; QUINOLINE; ANALOGS in [Li, Dandan; Oku, Naoya; Igarashi, Yasuhiro] Toyama Prefectural Univ, Biotechnol Res Ctr, 5180 Kurokawa, Imizu, Toyama 9390398, Japan; [Li, Dandan; Oku, Naoya; Igarashi, Yasuhiro] Toyama Prefectural Univ, Dept Biotechnol, 5180 Kurokawa, Imizu, Toyama 9390398, Japan; [Shinozaki, Yukiko] Toyama Coll, Natl Inst Technol, 13 Hongo Machi, Toyama, Toyama 9398630, Japan; [Kurokawa, Yoichi] Fukui Prefectural Univ, Dept Biosci & Biotechnol, Eiheiji Cho, Fukui, Japan in 2020, Cited 45. The Name is 4-Hydroxyquinolin-2(1H)-one. Through research, I have a further understanding and discovery of 86-95-3. Recommanded Product: 86-95-3

4-Hydroxy-3-methyl-2(1H)-quinolone (1), a molecule known for a long time and recently discovered from a Brassicaceae plant Isatis tinctoria without providing sufficient evidence to support the structure, was isolated from a fermentation extract of Burkholderia sp. 3Y-MMP isolated from a soil by a Zn2+ enrichment culture. Detailed spectroscopic analyses by MS and NMR, combined with C-13 chemical shift comparison with literature values of the related compounds and a synthetic preparation of 1, allowed its first full NMR characterization and identification of 2-quinolone but not 2-quinolinol (2) as the preferred tautomer for this heterocyclic system. While the metal-chelating activity was negligible, compound 1 at 10 mu M, a concentration lower than that in liquid production cultures, quenched hydroxy radical-induced chemiluminescence emitted by luminol by 86%. Because some Burkholderia species are pathogenic to plants and animals, the above result suggests that 1 is a potential antioxidant to counteract reactive oxygen species-based immune response in the host organisms.

About 4-Hydroxyquinolin-2(1H)-one, If you have any questions, you can contact Li, DD; Oku, N; Shinozaki, Y; Kurokawa, Y; Igarashi, Y or concate me.. Recommanded Product: 86-95-3

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles