Month: November 2022

Li, Ming published the artcileA study on the cataluminescence of propylene oxide on FeNi layered double hydroxides/graphene oxide, COA of Formula: C6H12O2, the publication is New Journal of Chemistry (2021), 45(26), 11823-11830, database is CAplus.

In this work, FeNi layered double hydroxides/graphene oxide (FeNi LDH/GO) was prepared, which exhibits excellent selective cataluminescent performance towards propylene oxide. The selectivity and sensitivity of the cataluminescence (CTL) reaction were investigated in detail. Moreover, the catalytic reaction mechanism, including the intermediate products and the conversion of reactants to products, was discussed based on both the exptl. and computational results. Furthermore, the proposed FeNi LDH/GO based CTL sensor was successfully applied for the determination of propylene oxide residue in fumigated raisins, which indicates extensive application potential for rapid food safety evaluation.

New Journal of Chemistry published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C6H12O2, COA of Formula: C6H12O2.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Du, Bin published the artcileStudy on catalytic synthesis of ethylene glycol cyclohexanone ketal by ferric solid superacid, Recommanded Product: 1,4-Dioxaspiro[4.5]decane, the publication is Liaoning Huagong (2012), 41(11), 1133-1135, database is CAplus.

Cyclohexanone ethylene glycol ketal was synthesized from cyclohexanone and ethylene glycol by using ferric solid superacid as the catalyst and cyclohexane as the water-carrying agent. The experiment results show that the ferric solid superacid has high activity and good stability; optimal synthesis conditions are as follows: molar ratio of cyclohexanone to ethylene glycol is 1:14, mass ratio of cyclohexanone to the catalyst is 32.8:1, volume ratio of cyclohexanone to cyclohexane is 2.08:1, and reaction time is 1 h. Under above conditions, the yield of cyclohexanone ethylene glycol ketal is over 86%.

Liaoning Huagong published new progress about 177-10-6. 177-10-6 belongs to dioxole, auxiliary class Dioxolane,Spiro, name is 1,4-Dioxaspiro[4.5]decane, and the molecular formula is C8H14O2, Recommanded Product: 1,4-Dioxaspiro[4.5]decane.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Qian, Deyun published the artcileGold(I)-catalyzed highly diastereo- and enantioselective alkyne oxidation/cyclopropanation of 1,6-enynes, Application of (R)-5,5′-Bis(diphenylphosphino)-2,2,2′,2′-tetrafluoro-4,4′-bi-1,3-benzodioxole, the publication is Angewandte Chemie, International Edition (2014), 53(50), 13751-13755, database is CAplus and MEDLINE.

A highly enantioselective oxidative cyclopropanation of 1,6-enynes catalyzed by cationic Au^I/chiral phosphoramidite complexes was presented. The new method provided convenient access to densely functionalized bicyclo[3.1.0]hexanes bearing three contiguous quaternary and tertiary stereogenic centers with high enantioselectivity (up to e.r. 98:2). Control experiments suggested that the quinoline moiety of the β-gold vinyloxyquinolinium intermediate in the reaction played an important role in promoting good enantioselectivity through a transitional auxiliary effect in the transition state.

Angewandte Chemie, International Edition published new progress about 503538-69-0. 503538-69-0 belongs to dioxole, auxiliary class (Atropisomeric Bisphosphine Ligands, name is (R)-5,5′-Bis(diphenylphosphino)-2,2,2′,2′-tetrafluoro-4,4′-bi-1,3-benzodioxole, and the molecular formula is C38H24F4O4P2, Application of (R)-5,5′-Bis(diphenylphosphino)-2,2,2′,2′-tetrafluoro-4,4′-bi-1,3-benzodioxole.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Kikuchi, Hiroto published the artcileActivity of host-derived attractants and their related compounds toward the zoospores of phytopathogenic Aphanomyces cochlioides, Computed Properties of 110204-45-0, the publication is Bioscience, Biotechnology, and Biochemistry (1995), 59(11), 2033-5, database is CAplus.

Eleven flavones, including cochliophilin A and a chromone, were chem. prepared to determine the attracting activity for zoospores of Aphanomyces cochlioides, a causative fungus of spinach root rot. Analyses of the structure-activity relationship of each revealed a significant correlation between the zoospore attracting activity and the A-ring oxygenation at C-5 and C-7 in flavone skeleton. The relative attractancy of 4 regioisomers of N-trans-feruloyl 4-O-methyldopamine, which was identified as a zoospore attractant specific to another host plant Chenopodium album, was also examined

Bioscience, Biotechnology, and Biochemistry published new progress about 110204-45-0. 110204-45-0 belongs to dioxole, auxiliary class Flavonoids, name is 9-Hydroxy-6-phenyl-8H-[1,3]dioxolo[4,5-g]chromen-8-one, and the molecular formula is C16H10O5, Computed Properties of 110204-45-0.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Zieba, Andrzej published the artcilePalladium-Catalysed Carboborylation for the Synthesis of Borylated Indanes, Synthetic Route of 503538-69-0, the publication is European Journal of Organic Chemistry (2021), 2021(29), 4072-4075, database is CAplus.

A palladium-catalyzed carboborylation reaction for the synthesis of borylated indanes has been investigated. This reaction proceeds in good yields with an achiral catalyst, and is tolerant of substitution on the aryl ring, although sensitivity to the substitution of the alkene was observed Initial studies towards an enantioselective version of this reaction were undertaken, identifying phosphoramidites as a promising ligand class. This allowed for the synthesis of chiral indane and indolone products with moderate levels of enantioselectivity.

European Journal of Organic Chemistry published new progress about 503538-69-0. 503538-69-0 belongs to dioxole, auxiliary class (Atropisomeric Bisphosphine Ligands, name is (R)-5,5′-Bis(diphenylphosphino)-2,2,2′,2′-tetrafluoro-4,4′-bi-1,3-benzodioxole, and the molecular formula is C10H14O, Synthetic Route of 503538-69-0.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Yang, Zhiwang published the artcilePreparation and application of SO₄^2-/SnO₂/SBA-15 solid acid catalyst for acetalization of cyclic ketones, Synthetic Route of 177-10-6, the publication is Cuihua Xuebao (2012), 33(5), 827-832, database is CAplus.

SO₄^2-/SnO₂/SBA-15 catalyst samples with different amounts of SnO₂ were prepared by a wetness impregnation method and characterized by X-ray diffraction, N₂ adsorption-desorption, and transmission electron microscopy. Their catalytic performance for the acetalization of 4-tert-butylcyclohexanone with glycol was investigated. The results showed that SBA-15 supported SO₄^2-/SnO₂ improved the catalytic activity markedly, which was caused by the increasing surface area of the sulfated tin oxide. The catalytic performance of SO₄^2-/20%SnO₂/SBA-15 for acetalization of several cyclic ketones with diols was also explored. Under the optimum conditions, a series of cyclic ketones such as cyclohexanone, 4-methylcyclohexanone, and 4-tert-butylcyclohexanone were well transformed into the corresponding products. The catalyst can be reused for several times without any significant loss in catalytic activity.

Cuihua Xuebao published new progress about 177-10-6. 177-10-6 belongs to dioxole, auxiliary class Dioxolane,Spiro, name is 1,4-Dioxaspiro[4.5]decane, and the molecular formula is C17H18N2O6, Synthetic Route of 177-10-6.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Hu, Jian published the artcilePalladium-Catalyzed Asymmetric Intermolecular Cyclization, Recommanded Product: (R)-5,5′-Bis(diphenylphosphino)-2,2,2′,2′-tetrafluoro-4,4′-bi-1,3-benzodioxole, the publication is Angewandte Chemie, International Edition (2013), 52(33), 8676-8680, database is CAplus and MEDLINE.

The palladium(II)-catalyzed domino Heck cyclization reactions of o-vinylaryl triflates with cyclic alkenes to give polycyclic products, e.g., I, with high enantioselectivity was reported. The methodol. was applied to a short synthesis of diamine II, a precursor of (-)-martinellic acid.

Angewandte Chemie, International Edition published new progress about 503538-69-0. 503538-69-0 belongs to dioxole, auxiliary class (Atropisomeric Bisphosphine Ligands, name is (R)-5,5′-Bis(diphenylphosphino)-2,2,2′,2′-tetrafluoro-4,4′-bi-1,3-benzodioxole, and the molecular formula is C38H24F4O4P2, Recommanded Product: (R)-5,5′-Bis(diphenylphosphino)-2,2,2′,2′-tetrafluoro-4,4′-bi-1,3-benzodioxole.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Maj, Anna M. published the artcileFirst catalytic asymmetric hydrogenation of quinoxaline-2-carboxylates, Synthetic Route of 503538-69-0, the publication is Tetrahedron (2016), 72(10), 1375-1380, database is CAplus.

For the first time, the asym. hydrogenation of quinoxaline-2-carboxylates was performed successfully. The best catalysts are based on iridium complexes modified by chiral phosphorous ligands. Accelerated examination of ligands and catalysts has been undertaken by using a Chemspeed workstation (automated instrument) workstation enables carrying out, in parallel, eight independent catalytic reactions at the laboratory scale. Tetrahydroquinoxaline-2-carboxylates could be obtained with high yields and up to 74% ee. The synthesis of the target compounds was achieved using chiral ligands, such as (11aR)-10,11,12,13-tetrahydro-N,N-dimethyldiindeno[7,1-de:1′,7′-fg][1,3,2]dioxaphosphocin-5-amine [i/e/. (R)-siphos], 1,1′-[(1S)-6,6′-dimethoxy[1,1′-biphenyl]-2,2′-diyl]bis[1,1-diphenylphosphine] [i.e., (S)-MeO-BIPHEP], (R)-Cl-MeO-BIPHEP, (R)-difluorphos, (R)-GARPHOS, (R)-P-PHOS, (S)-C3-TUNEPHOS [i.e., 1,1′-[(13aS)-7,8-dihydro-6H-dibenzo[f,h][1,5]dioxonin-1,13-diyl]bis[1,1-diphenylphosphine]], (S)-SEGPHOS, (S)-Xyl-SolPhos, CATASium T3, N-[(1R)-2-[(11bR)-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-yloxy]-1-methylethyl]-N‘-phenylurea [i.e., ureaphos], SL-J404-1, SL-J006-1, SL-J002-1, SL-J003-1, SL-J009-1, SL-T002-1, SL-W006-1. Pre-catalysts included bis(acetato-κO,κO‘)[(4R)-1,1′-[4,4′-bi-1,3-benzodioxole]-5,5′-diylbis[1,1-diphenylphosphine-κP]]ruthenium [i.e., Ru(OAc)₂[(R)-segphos]], [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2,3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]ruthenium [i.e., RuCl[(R,R)-TsDPEN][p-cymene]] and [1,1′-(1S)-[4,4′-bi-1,3-benzodioxole]-5,5′-diylbis[1,1-diphenylphosphine-κP]][4-cyano-3-nitrobenzenecarboxylato(2-)-κC⁶,κO¹](η³-2-propen-1-yl)iridium.

Tetrahedron published new progress about 503538-69-0. 503538-69-0 belongs to dioxole, auxiliary class (Atropisomeric Bisphosphine Ligands, name is (R)-5,5′-Bis(diphenylphosphino)-2,2,2′,2′-tetrafluoro-4,4′-bi-1,3-benzodioxole, and the molecular formula is C38H24F4O4P2, Synthetic Route of 503538-69-0.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Berkelhamer, Sara K. published the artcileIn vitro consequences of electronic-cigarette flavoring exposure on the immature lung, COA of Formula: C11H14O4, the publication is International Journal of Environmental Research and Public Health (2019), 16(19), 3635, database is CAplus and MEDLINE.

The developing lung is uniquely susceptible and may be at increased risk of injury with exposure to e-cigarette constituents. We hypothesize that cellular toxicity and airway and vascular responses with exposure to flavored refill solutions may be altered in the immature lung. Fetal, neonatal, and adult ovine pulmonary artery smooth muscle cells (PASMC) were exposed to popular flavored nicotine-free e-cigarette refill solutions (menthol, strawberry, tobacco, and vanilla) and unflavored solvents: propylene glycol (PG) or vegetable glycerin (VG). Viability was assessed by lactate dehydrogenase assay. Brochodilation and vasoreactivity were determined on isolated ovine bronchial rings (BR) and pulmonary arteries (PA). Neither PG or VG impacted viability of immature or adult cells; however, exposure to menthol and strawberry flavored solutions increased cell death. Neonatal cells were uniquely susceptible to menthol flavoring-induced toxicity, and all four flavorings demonstrated lower LDs (LD50) in immature PASMC. Exposure to flavored solutions induced bronchodilation of neonatal BR, while only menthol induced airway relaxation in adults. In contrast, PG/VG and flavored solutions did not impact vasoreactivity with the exception of menthol-induced relaxation of adult PAs. The immature lung is uniquely susceptible to cellular toxicity and altered airway responses with exposure to common flavored e-cigarette solutions

International Journal of Environmental Research and Public Health published new progress about 68527-74-2. 68527-74-2 belongs to dioxole, auxiliary class Dioxolane,Benzene,Phenol,Ether, name is 2-Methoxy-4-(4-methyl-1,3-dioxolan-2-yl)phenol, and the molecular formula is C11H14O4, COA of Formula: C11H14O4.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Islam, Tofazzal Md. published the artcileInterruption of the homing events of phytopathogenic Aphanomyces cochlioides zoospores by secondary metabolites from nonhost Amaranthus gangeticus, Name: 9-Hydroxy-6-phenyl-8H-[1,3]dioxolo[4,5-g]chromen-8-one, the publication is Journal of Pesticide Science (Tokyo, Japan) (2004), 29(1), 6-14, database is CAplus.

On the screening of 200 nonhost plants, an Amaranthus gangeticus extract was found to attract and subsequently inhibit the motility of Aphanomyces cochlioides zoospores. The attractant was identified as N-trans-feruloyl-4-O-methyldopamine (I) and the motility inhibitor as nicotinamide (II) using bioassay-guided fractionation and spectroscopic methods. Also isolated were cochliophilin A and chondrillasterol 3-O-β-D-glucopyranoside. I had no inhibitory effect on zoospore motility whereas II immediately halted the motility and caused encystment in a dose-dependent manner (MIC, 5 × 10^-8 M). The cystospores produced by II regenerated zoospores instead of germinating. Concomitant application of I and II produced cystospores that germinated to give hyphae. TLC examinations revealed that A. gangeticus seedling exuded sufficient amounts of II from the roots. Exudation of II from A. gangeticus might be involved in its resistance against the soilborne oomycete phytopathogen A. cochlioides.

Journal of Pesticide Science (Tokyo, Japan) published new progress about 110204-45-0. 110204-45-0 belongs to dioxole, auxiliary class Flavonoids, name is 9-Hydroxy-6-phenyl-8H-[1,3]dioxolo[4,5-g]chromen-8-one, and the molecular formula is C16H10O5, Name: 9-Hydroxy-6-phenyl-8H-[1,3]dioxolo[4,5-g]chromen-8-one.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem