Esters-buliding-blocks

Demarteau, Jeremy published the artcileAminolytic upcycling of poly(ethylene terephthalate) wastes using a thermally-stable organocatalyst, Application In Synthesis of 627-93-0, the publication is Polymer Chemistry (2020), 11(30), 4875-4882, database is CAplus.

Poly(ethylene terephthalate) (PET) is one of the most commonly used plastics for a wide range of applications, but is also one on the main contributors to the accumulation of plastic waste in the environment. Herein, we propose an aminolytic method to depolymerise PET using various amino-alcs. by organocatalysis and their subsequent use for the production of poly(ester-amide)s. This research aims to highlight the potential of thermally stable acid-base mixtures for depolymerization of PET in the presence of amines, specifically TBD : MSA. The chemoselectivity of the process favors the formation of diol terephthalamides in high yields. Different amino alcs. are also explored in order to obtain diols with secondary amine or ether functionalities. Finally, these novel terephthalamide diols are investigated as novel synthons for the synthesis of poly(ester-amide)s, showing potential for the “creative reuse” of plastic wastes.

Polymer Chemistry published new progress about 627-93-0. 627-93-0 belongs to esters-buliding-blocks, auxiliary class Ploymers, name is Dimethyl adipate, and the molecular formula is C8H14O4, Application In Synthesis of 627-93-0.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Kus, Piotr M. published the artcileDevelopment of supercritical CO₂ extraction of bioactive phytochemicals from black poplar (Populus nigra L.) buds followed by GC-MS and UHPLC-DAD-QqTOF-MS, Related Products of esters-buliding-blocks, the publication is Journal of Pharmaceutical and Biomedical Analysis (2018), 15-27, database is CAplus and MEDLINE.

The supercritical CO₂ (SC-CO₂) extraction process of black poplar (Populus nigra L.) buds was optimized (pressure, temperature) based on the yields of major phytochems. (volatiles and non-volatiles). The optimal settings were 30 MPa/60°C. Major volatiles determined by GC-MS in the optimized SC-CO₂ extract (mg of benzyl salicylate equivalent (BSE) per 100 g of buds) were: pinostrobin chalcone (1574.2), β-eudesmol (640.8), α-eudesmol (581.9), 2-methyl-2-butenyl-p-coumarate (289.9), pentyl-p-coumarate (457.0), γ-eudesmol (294.4), and benzyl salicylate (289.2). Partial qual. similarity was observed between SC-CO₂ extracts and corresponding hydrodistd. essential oil dominated by sesquiterpenes, but with lower yields. Major compounds (mg per 100 g of buds) identified by UHPLC-DAD-QqTOF-MS in the optimized SC-CO₂ extract were: pinostrobin (751.7), pinocembrin (485.6), 3-O-pinobanksin acetate and methyl-butenyl-p-coumarate (290.2; 144.9 of pinobanksin and p-coumaric acid equivalent, resp.). SC-CO₂ extraction was found useful for green, efficient and simultaneous extraction of both volatile/non-volatile, bioactive phytochems. of poplar buds – precursors of poplar-type propolis.

Journal of Pharmaceutical and Biomedical Analysis published new progress about 5205-11-8. 5205-11-8 belongs to esters-buliding-blocks, auxiliary class Alkenyl,Benzene,Ester, name is 3-Methylbut-2-en-1-yl benzoate, and the molecular formula is C12H14O2, Related Products of esters-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Maekawa, Hirofumi published the artcileReductive carboxylation of aromatic esters by electron transfer from magnesium metal, Recommanded Product: Ethyl 3,5-difluorobenzoate, the publication is Tetrahedron Letters (2017), 58(3), 206-209, database is CAplus.

Magnesium-promoted reductive carboxylation of Et benzoates in the presence of chlorotrimethylsilane in N,N-dimethylformamide brought about a new carbon-carbon bond formation between the carbonyl carbon atom and carbon dioxide to give the corresponding benzoylformic acids in good yield. It is noteworthy that only Et benzoates with substituents at the meta-position were converted into benzoylformic acid derivatives Moreover, no mandelic acid was detected even under the reductive conditions. This result indicates that benzoylformic acid was obtained after hydrolysis of a carboxylated intermediate, which would exist as a stabilized structure in the reaction media.

Tetrahedron Letters published new progress about 350-19-6. 350-19-6 belongs to esters-buliding-blocks, auxiliary class Fluoride,Benzene,Ester, name is Ethyl 3,5-difluorobenzoate, and the molecular formula is C9H8F2O2, Recommanded Product: Ethyl 3,5-difluorobenzoate.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Oki, Yoshitaka published the artcileSynthesis of AB and ABA type block copolymers of vinyl chloride using iniferter technique, Formula: C12H17NS2, the publication is Polymer Journal (Tokyo, Japan) (2002), 34(10), 736-741, database is CAplus.

The photopolymerization of vinyl chloride (VC) with benzyl N,N-diethyldithiocarbamate (BDC) or p-xylylene bis(N,N-diethyldithiocarbamate) (XDC) was carried out in 1,2-dichloroethane at 30°C. From the ¹H NMR spectra, these poly(vinyl chloride)s (PVC) were found to contain mono- or di-functional polymers which can be used for synthesizing the AB type or ABA type block copolymers, resp. The photocopolymn. of the mono-functional PVC with styrene (St) or vinyl acetate (VAc) was carried out in cyclohexanone at 30°C. The obtained copolymers were the AB type block copolymers of VC with St or VAc. The photocopolymn. of the di-functional PVC with St in cyclohexanone at 30°C gave an ABA type block copolymer of VC and St.

Polymer Journal (Tokyo, Japan) published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C12H17NS2, Formula: C12H17NS2.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Hamada, Tomohito published the artcileImproved Synthesis of Unsymmetrical Carbonate Derivatives Using Calcium Salts, Product Details of C5H7F3O3, the publication is Organic Process Research & Development (2019), 23(4), 667-673, database is CAplus.

An effective synthetic method for unsym. carbonate species has been developed. Calcium oxide and calcium hydroxide were found to be highly effective for this reaction, affording unsym. carbonates in high yield and purity. Calcium chloride, which is a coproduct, serves as a water scavenger that can be easily removed. Addnl. drying processes and complicated purification steps are not necessary in this reaction. This improved process is important in terms of green sustainable chem. principles.

Organic Process Research & Development published new progress about 156783-96-9. 156783-96-9 belongs to esters-buliding-blocks, auxiliary class Trifluoromethylated Building Blocks, name is Ethyl (2,2,2-trifluoroethyl) carbonate, and the molecular formula is C5H7F3O3, Product Details of C5H7F3O3.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Sakai, Kentaro published the artcileA Germanium Catalyst Accelerates the Photoredox α-C(sp³)-H Alkylation of Primary Amines, Name: Dimethyl itaconate, the publication is Organic Letters (2022), 24(18), 3325-3330, database is CAplus and MEDLINE.

Site-selective C(sp³)-H functionalizations using photoredox catalysis (PC) and hydrogen atom transfer (HAT) catalysis have received increasing attention. Here, a Ph₂GeCl₂ cocatalyst that greatly improves the yield of αC(sp³)-H alkylation of primary amines e.g., 3-phenylpropan-1-amine catalyzed by a PC-HAT hybrid system has been reported. The α-position of the amino group selectively reacted even when weaker C-H bonds existed in the substrates. This finding may help the design of a novel site-selective hybrid catalysis.

Organic Letters published new progress about 617-52-7. 617-52-7 belongs to esters-buliding-blocks, auxiliary class Alkenyl,Aliphatic hydrocarbon chain,Ester, name is Dimethyl itaconate, and the molecular formula is C7H10O4, Name: Dimethyl itaconate.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Yoshimi, Yasuo published the artcileSize of heparin-imprinted nanoparticles reflects the matched interactions with the target molecule, Name: Benzyl diethylcarbamodithioate, the publication is Sensors (2019), 19(10), 2415, database is CAplus and MEDLINE.

It has been shown that the faradic current at an electrode grafted with molecularly imprinted polymer (MIP) is sensitive to the specific target mol. used as the template. This phenomenon is applicable to sensors with very high selectivity, but the sensing mechanism is still a black box. We investigated the size sensitivity of nanoparticles of molecularly imprinted polymers (MIP-NPs) to a specific interaction for determination of the mechanism of the gate effect and its feasibility for new applications. Nanoparticles of poly(methacryloxy Et trimethylammonium chloride-co-acrylamide-co-methylenebisacrylamide) imprinted with heparin immobilized on glass beads were synthesized. The diameter of the MIP-NPs of heparin was increased by the presence of the heparin template but was insensitive to chondroitin sulfate C (CSC), the analog of heparin. The high selectivity of the MIP-NPs was consistent with the selectivity of electrodes grafted with a heparin-imprinted polymer in our previous studies. The quartz crystal microbalance probes immobilizing heparin or CSC were sensitive to MIP-NPs, which indicates that the binding ability of MIP-NP does not discriminate between the template and other glycosaminoglycans. These results indicate that the size of the MIP-NP is sensitive to the matched binding with the template through the imprinted cavity.

Sensors published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C4Br2N2O4S, Name: Benzyl diethylcarbamodithioate.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Kurouchi, Hiroaki published the artcileSynthesis of Medium-Ring-sized Benzolactams by Using Strong Electrophiles and Quantitative Evaluation of Ring-size Dependency of the Cyclization Reaction Rate, Name: Dimethyl adipate, the publication is Journal of Organic Chemistry (2020), 85(2), 876-901, database is CAplus and MEDLINE.

Benzolactams with medium-sized rings were synthesized via electrophilic aromatic substitution reaction of carbamoyl cations (R₁R₂N⁺=C=O) in good to high yields without dilution These reactions were utilized to quant. examine the extent of retardation of medium-sized ring formation, compared to 5- or 6-membered ring formation. The order of reaction rates of formation of cyclic benzolactams is 6- > 5- > 7- > 8- > 9-membered ring at 25°. The present reaction provides a route to 8- and 9-membered benzolactams.

Journal of Organic Chemistry published new progress about 627-93-0. 627-93-0 belongs to esters-buliding-blocks, auxiliary class Ploymers, name is Dimethyl adipate, and the molecular formula is C8H14O4, Name: Dimethyl adipate.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Ishizu, Koji published the artcileKinetics of Hyperbranched Polystyrenes by Free Radical Polymerization of Photofunctional Inimer, Application In Synthesis of 3052-61-7, the publication is Macromolecules (2002), 35(9), 3781-3784, database is CAplus.

Kinetics of hyperbranched polystyrene was studied by free radical polymerization of photofunctional inimer CH₂=CH-p-C₆H₄-CH₂SC(S)N(Et)₂. The degree of branching was also studied. Results demonstrated that d. functional theory calculations provide a reliable and quant. prediction of exptl. observed trends in C-S bond dissociation energies for several model compounds

Macromolecules published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C12H17NS2, Application In Synthesis of 3052-61-7.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Ishizu, Koji published the artcileDegree of branching of hyperbranched polystyrenes via a controlled radical mechanism of an inimer: Determination by a kinetic approach, Computed Properties of 3052-61-7, the publication is Journal of Applied Polymer Science (2005), 96(5), 1810-1815, database is CAplus.

We studied, with a kinetic approach, the living nature and degree of branching (DB) of the formation of hyperbranched polystyrene by the free-radical photopolymerization of 2-(N,N-diethyldithiocarbamyl)methylstyrene in benzene. The free-radical polymerization proceeded with a living radical mechanism. Subsequently, we treated the kinetics of the initiation and propagation steps of the active A* and B* (side-group) sites with model compounds The degradation rates of two types of dithiocarbamate groups at the A and B sites agreed well with theor. trends for C-S bond dissociation energies predicted by the d. functional theory for model compounds The reactivity of the initiating B* groups was greater than that of the propagating A* groups. DB of the hyperbranched polymers was estimated to be 0.31 with both reaction rates in terms of Mueller’s equation. This result supported the DB value (0.39) estimated from NMR data. The hyperbranched mols. obtained in this work were not perfectly dendritic but had somewhat defective structures.

Journal of Applied Polymer Science published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C12H17NS2, Computed Properties of 3052-61-7.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics