Category: benzofurans

In 2020 CHEM COMMUN published article about NADH MODEL COMPOUNDS; ASYMMETRIC REDUCTION; CHIRAL 1,4-DIHYDROPYRIDINES; PYRIDINIUM SALTS; HYDRIDE TRANSFER; OXIDATION in [Ogawa, Narihito; Kosugi, Yuya; Takazawa, Takayuki] Meiji Univ, Dept Appl Chem, Kawasaki, Kanagawa 2148571, Japan; [Furukawa, Sei; Kanomata, Nobuhiro] Waseda Univ, Dept Chem & Biochem, Shinjuku Ku, Tokyo 1698555, Japan in 2020, Cited 22. The Name is Isobenzofuran-1(3H)-one. Through research, I have a further understanding and discovery of 87-41-2. Category: benzofurans

Magnesium hemithioacetates were used as model cysteine compounds to mimic natural hemithioacetals, and their biomimetic oxidation reactions using a model NAD(+) compound were investigated. Cyclic hemithioacetate was found to be the best substrate for the reaction with the model NAD(+) compound, which gave the corresponding NADH analog in excellent yield.

Category: benzofurans. Welcome to talk about 87-41-2, If you have any questions, you can contact Ogawa, N; Furukawa, S; Kosugi, Y; Takazawa, T; Kanomata, N or send Email.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

An article Synthesis and Photodimerization of 2-and 2,3-Disubstituted Anthracenes: Influence of Steric Interactions and London Dispersion on Diastereoselectivity WOS:000481979200026 published article about CATALYZES ALDOL-CONDENSATIONS; 2,3-DIMETHYLENEBUTADIENE DIANION; CONVENIENT SYNTHESIS; MOLECULAR-STRUCTURE; EFFICIENT SYNTHESIS; PHOTO-DIMERIZATION; CRYSTAL-STRUCTURE; ISOBENZOFURAN; PHOTOCHEMISTRY; 9-TERT-BUTYLANTHRACENE in [Geiger, Thomas; Haupt, Anne; Bettinger, Holger F.] Eberhard Karls Univ Tubingen, Inst Organ Chem, Morgenstelle 18, D-72076 Tubingen, Germany; [Maichle-Moessmer, Caecilia; Schrenk, Claudio; Schnepf, Andreas] Eberhard Karls Univ Tubingen, Inst Anorgan Chem, Morgenstelle 18, D-72076 Tubingen, Germany in 2019, Cited 84. Quality Control of Isobenzofuran-1(3H)-one. The Name is Isobenzofuran-1(3H)-one. Through research, I have a further understanding and discovery of 87-41-2

There is increased evidence that the effect of bulky groups in organic, organometallic, and inorganic chemistry is not only repulsive but can be attractive because of London dispersion interactions. The influence of the size of primary alkyl substituents in 2- ‘ and 2,3-positions of anthracenes on the diastereoselectivity (anti vs syn dimer) of the [pi(4s) + pi(4s)] photoinduced dimerization is investigated. The synthesis of the anthracene derivatives was achieved by Suzuki-Miyaura reaction of 2,3-dibromoanthracene with alkylboronic acids as well as by reduction of anthraquinones that were obtained from 2,3-disubstituted 1,3-butadienes and naphthoquinone followed by dehydrogenation. The mixtures of dianthracene isomers were analyzed with respect to the anti/syn-ratio of the products by X-ray crystallography and nuclear Overhauser effect spectroscopy. While for the 2,3-dimethylanthracene the anti and syn isomers were formed in equal amounts, the anti dimers are the major products in all other cases. A linear correlation (R-2 = 0.98) between the steric size (Charton parameter) and the isomeric ratio suggests that the selectivity is dominated by classical repulsive steric effects. An exception is the iso-butyl substituent that produces an increased amount of the syn isomer. It is suggested that this is due to an exalted effect of London dispersion interactions.

Quality Control of Isobenzofuran-1(3H)-one. Welcome to talk about 87-41-2, If you have any questions, you can contact Geiger, T; Haupt, A; Maichle-Mossmer, C; Schrenk, C; Schnepf, A; Bettinger, HF or send Email.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

Product Details of 87-41-2. In 2019 SCI TOTAL ENVIRON published article about POLYCYCLIC AROMATIC-HYDROCARBONS; MICROBIAL COMMUNITY; MASS-SPECTROMETRY; PHOSPHORUS SOLUBILIZATION; FUSARIUM-WILT; SOIL; GROWTH; MICROORGANISMS; RHIZOSPHERE; PSEUDOMONAS in [Yu, Le-Yi; Huang, He-Biao; Wang, Xiao-Hong; Li, Sha; Feng, Nai-Xian; Zhao, Hai-Ming; Huang, Xian-Pei; Li, Yan-Wen; Li, Hui; Cai, Quan-Ying; Mo, Ce-Hui] Jinan Univ, Coll Life Sci & Technol, Guangdong Prov Res Ctr Environm Pollut Control &, Guangzhou 510632, Guangdong, Peoples R China in 2019, Cited 73. The Name is Isobenzofuran-1(3H)-one. Through research, I have a further understanding and discovery of 87-41-2.

A great amount of insoluble phosphate in agricultural soils is not available for crops. Three strains of bacteria (Bacillus megaterium YLYP1 Pseudumonas prosekii YLYP6 and Pseudomonas sp. YLYP29) isolated from activated sludge and soil could efficiently solubilise tricalcium phosphate. In particular, the novel strain P. prosekii YLYP6 produced 716 mg L-1 of available phosphate within 6 days under the optimal culture conditions [20 degrees C, pH 7.9, inoculum size of 0.5% (v:v)] determined by response surface methodology. P. prosekii YLYP6 demonstrated efficient phosphate solubilisation in response to broad variations in pH (5-9) and temperature (15-35 degrees C). The phosphate solubilisation curves of the strains fit well with a first-order kinetic model (R-2 > 0.939), with a halt-life of 1.51-5.94 d for 5.0 g L-1 calcium phosphate. Continuous culture experiments combined with scanning electron microscopic observations and gas chromatography-mass spectrometry analysis revealed that 2,3-dimethylfumaric acid, gluconic and N-butyl-tert-butylamine that were produced by P. prosekii YLYP6 were responsible for phosphate solubilisation by supplying H+ ions and organic anions. Efficient phosphate solubilisation in actual soil by P. prosekii YLYP6 demonstrated the strong application potential to reduce the use of chemical P fertilisers and the resulting agricultural nonpoint pollution. (C) 2018 Elsevier B.V. All rights reserved.

Welcome to talk about 87-41-2, If you have any questions, you can contact Yu, LY; Huang, HB; Wang, XH; Li, S; Feng, NX; Zhao, HM; Huang, XP; Li, YW; Li, H; Cai, QY; Mo, CH or send Email.. Product Details of 87-41-2

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

Recommanded Product: 87-41-2. I found the field of Chemistry very interesting. Saw the article Platinum-on-Carbon-Catalyzed Aqueous Oxidative Lactonization of Diols by Using Molecular Oxygen published in 2019, Reprint Addresses Sajiki, H; Sawama, Y (corresponding author), Gifu Pharmaceut Univ, Lab Organ Chem, 1-25-4 Daigaku Nishi, Gifu 5011196, Japan.. The CAS is 87-41-2. Through research, I have a further understanding and discovery of Isobenzofuran-1(3H)-one.

A lactonization of various diols catalyzed by platinum on carbon (Pt/C) in water under an atmosphere of molecular oxygen was developed. Derivatives of 1,4- 1,5- and 1,6-diols were transformed into the corresponding five-, six-, and seven-membered lactones by the present oxidative lactonization method.

Recommanded Product: 87-41-2. Welcome to talk about 87-41-2, If you have any questions, you can contact Takakura, R; Ban, K; Sajiki, H; Sawama, Y or send Email.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

Category: benzofurans. I found the field of Chemistry very interesting. Saw the article Platinum-on-Carbon-Catalyzed Aqueous Oxidative Lactonization of Diols by Using Molecular Oxygen published in 2019, Reprint Addresses Sajiki, H; Sawama, Y (corresponding author), Gifu Pharmaceut Univ, Lab Organ Chem, 1-25-4 Daigaku Nishi, Gifu 5011196, Japan.. The CAS is 87-41-2. Through research, I have a further understanding and discovery of Isobenzofuran-1(3H)-one.

A lactonization of various diols catalyzed by platinum on carbon (Pt/C) in water under an atmosphere of molecular oxygen was developed. Derivatives of 1,4- 1,5- and 1,6-diols were transformed into the corresponding five-, six-, and seven-membered lactones by the present oxidative lactonization method.

Category: benzofurans. Bye, fridends, I hope you can learn more about C8H6O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

Authors Jiang, XL; Zhang, JH; Zhao, DM; Li, YH in ROYAL SOC CHEMISTRY published article about ACCEPTORLESS DEHYDROGENATION; ALIPHATIC-ALCOHOLS; COMPLEXES; OXIDATION; ESTERIFICATION in [Jiang, Xiaolin; Zhao, Dongmei] Shenyang Pharmaceut Univ, Minist Educ, Key Lab Struct Based Drug Design & Discovery, Shenyang 110016, Peoples R China; [Jiang, Xiaolin; Zhang, Jiahui; Li, Yuehui] Chinese Acad Sci, State Key Lab Oxo Synth & Select Oxidat, Lanzhou Inst Chem Phys, Suzhou Res Inst LICP, Lanzhou 730000, Peoples R China; [Zhang, Jiahui] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450001, Henan, Peoples R China in 2019, Cited 25. Formula: C8H6O2. The Name is Isobenzofuran-1(3H)-one. Through research, I have a further understanding and discovery of 87-41-2

The presence of different aldehydes is found to have a significant influence on the catalytic performance when using PN(H)P type ligands for dehydrogenation of alcohols. Accordingly, hybrid multi-dentate ligands were discovered based on an oxygen-transfer alkylation of PNP ligands by aldehydes. The relevant Ru-PNN(PO) system provided the desired unsymmetrical esters in good yields via acceptorless dehydrogenation of alcohols. Hydrogen bonding interactions between the phosphine oxide moieties and alcohol substrates likely assisted the observed high chemoselectivity.

Formula: C8H6O2. Bye, fridends, I hope you can learn more about C8H6O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

Recommanded Product: 87-41-2. Recently I am researching about ONE-STEP SYNTHESIS; BENZOIC-ACIDS; CARBOXYLIC-ACIDS; SOFT ACIDS; OXIDASE CATALYSIS; INTERNAL ALKYNES; H ALKENYLATIONS; BASES HSAB; ALDEHYDES; KETONES, Saw an article supported by the University of the Ryukyus. Published in MDPI in BASEL ,Authors: Renzetti, A; Fukumoto, K. The CAS is 87-41-2. Through research, I have a further understanding and discovery of Isobenzofuran-1(3H)-one

Phthalides and ,-butenolides are two related classes of oxygenated heterocycles with a wide range of biological activities. An innovative strategy to prepare these compounds is based on CH bond functionalization reactions, in which two simple, unfunctionalized molecules are coupled together with cleavage of a CH bond and formation of a CX bond (X=C or heteroatom). This paper reviews the methods for the synthesis of phthalides and ,-butenolides by CH bond functionalization from non-halogenated starting materials. Over 30 methods are reported, mostly developed during the past ten years.

Recommanded Product: 87-41-2. Welcome to talk about 87-41-2, If you have any questions, you can contact Renzetti, A; Fukumoto, K or send Email.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

Recommanded Product: Isobenzofuran-1(3H)-one. In 2019 PHYS CHEM CHEM PHYS published article about OXIDATIVE DEHYDROGENATION; CARBON NANOTUBES; LIQUID-PHASE; EFFICIENT; GRAPHENE; HYDROGENATION; CARBOCATALYST; NITROARENES; OXIDE; BN in [Wu, Shuchang] Taizhou Univ, Sch Pharmaceut & Mat Engn, Taizhou 318000, Zhejiang, Peoples R China; [Lin, Yangming; Wen, Guodong; Liu, Hongyang; Su, Dang Sheng] Chinese Acad Sci, Shenyang Natl Lab Mat Sci, Inst Met Res, 72 Wenhua Rd, Shenyang 110016, Peoples R China; [Zhong, Bingwei] Zhejiang A&F Univ, JiYang Coll, 77 Puyang Rd, Zhuji 311800, Peoples R China in 2019, Cited 28. The Name is Isobenzofuran-1(3H)-one. Through research, I have a further understanding and discovery of 87-41-2.

A zigzag-type quinone performs better than an armchair-type quinone in the reduction of nitrobenzene. When different kinds of functionalities co-exist, the reaction is dominated by the most active sites, but the most negative sites should also be taken into consideration if the acitive sites have zigzag structures.

Recommanded Product: Isobenzofuran-1(3H)-one. Bye, fridends, I hope you can learn more about C8H6O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

Formula: C8H6O2. In 2019 ORGANOMETALLICS published article about N-HETEROCYCLIC CARBENE; EFFICIENT CATALYSTS; BASIS-SETS; SELECTIVE HYDROGENATION; MOLECULAR CALCULATIONS; CARBOXYLIC ESTERS; COMPLEXES; ALCOHOLS; REDUCTION; ACID in [Linh Le; Liu, Jiachen; He, Tianyi; Malek, Jack C.; Cervarich, Tia N.; Buttner, John C.; Pham, John; Keith, Jason M.; Chianese, Anthony R.] Colgate Univ, Dept Chem, 13 Oak Dr, Hamilton, NY 13346 USA in 2019, Cited 68. The Name is Isobenzofuran-1(3H)-one. Through research, I have a further understanding and discovery of 87-41-2.

We report the conversion of a series of CNN-pincer-ruthenium complexes Ru(CNN)HCl(CO) to a CC-chelated form Ru(CC)(PR3)(2)H(CO) on reaction with sodium tert-butoxide and monodentate phosphines. When the phosphine is triphenylphosphine, cis-phosphine complexes form at room temperature, which convert to the trans isomer at elevated temperatures. When the phosphine is tricyclohexylphosphine, only the trans-phosphine isomer is observed. The CC-chelated complexes are active catalysts for the hydrogenation of esters, without the need for added base. The ligand structure-activity relationship in the series of CC-chelated complexes mirrors that in the precursor CNN-Ru complexes, potentially indicating a common catalytic mechanism. Density functional theory calculations establish a plausible mechanism for the CNN-to-CC rearrangement and demonstrate that this rearrangement is potentially reversible under the conditions of ester hydrogenation catalysis.

Welcome to talk about 87-41-2, If you have any questions, you can contact Le, L; Liu, JC; He, TY; Malek, JC; Cervarich, TN; Buttner, JC; Pham, J; Keith, JM; Chianese, AR or send Email.. Formula: C8H6O2

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem

Product Details of 87-41-2. Qian, SQ; Li, ZQ; Li, MY; Wisniewski, SR; Qiao, JX; Richter, JM; Ewing, WR; Eastgate, MD; Chen, JS; Yu, JQ in [Qian, Shaoqun; Li, Zi-Qi; Li, Minyan; Yu, Jin-Quan] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA; [Wisniewski, Steven R.; Eastgate, Martin D.] Bristol Myers Squibb, Chem & Synthet Dev, New Brunswick, NJ 08903 USA; [Chen, Jason S.] Scripps Res Inst, Automated Synth Facil, La Jolla, CA 92037 USA; [Qiao, Jennifer Xiaoxin; Ewing, William R.] Bristol Myers Squibb, Discovery Chem, Princeton, NJ 08543 USA; [Richter, Jeremy M.] Bristol Myers Squibb, Res & Dev, Hopewell, NJ 08534 USA published Ligand-Enabled Pd(II)-Catalyzed C(sp(3))-H Lactonization Using Molecular Oxygen as Oxidant in 2020, Cited 41. The Name is Isobenzofuran-1(3H)-one. Through research, I have a further understanding and discovery of 87-41-2.

Pd(II)-catalyzed C-H lactonization of o-methyl benzoic acid substrates has been achieved using molecular oxygen as the oxidant. This finding provides a rare example of C-H oxygenation through Pd(II)/Pd(0) catalysis as well as a method to construct biologically important benzolactone scaffolds. The use of a gas mixture of 5% oxygen in nitrogen demonstrated the possibility for its application in pharmaceutical manufacturing.

Welcome to talk about 87-41-2, If you have any questions, you can contact Qian, SQ; Li, ZQ; Li, MY; Wisniewski, SR; Qiao, JX; Richter, JM; Ewing, WR; Eastgate, MD; Chen, JS; Yu, JQ or send Email.. Product Details of 87-41-2

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem