Category: 517-23-7

Taib, Layla Ahmed published the artcileSolvent-free synthesis of 4-substituted coumarins catalyzed by novel Bronsted acidic ionic liquids with perchlorate anion: a convenient and practical complementary method for pechmann condensation, Safety of 3-Acetyldihydrofuran-2(3H)-one, the publication is Reaction Kinetics, Mechanisms and Catalysis (2021), 133(1), 383-403, database is CAplus.

Herein, three novel sulfonic-functionalized Bronsted acidic ionic liquids containing perchlorate anion counterparts e.g., I were prepared These ionic liquid catalysts e.g., I were prepared through simple and ecofriendly procedures and then applied as efficient catalysts with high yields under solvent-free conditions for the synthesis of 4-substituted coumarins e.g., II through the Pechmann condensation of different phenols e.g., naphthalen-1-ol and β-ketoesters R(O)CH(R¹)C(O)OR² [R = Me, Ph; R¹ = H; R² = Et; R¹R² = -(CH₂)₂-]. Compared to previous works, the proposed method offers several benefits, such as cleaner reactions, decreased reaction times, high yields, and the lack of laborious workup or purification procedures. Particularly, these catalysts make the condensation of less activated phenols feasible. Besides the described benefits, this advanced protocol was applied successfully for the synthesis of coumarins e.g., III from γ-lactone as 3-acetyldihydrofuran-2(3H)-one. The simplicity in operation, applicability and feasibility of this protocol for diverse substrates make it an efficient alternative to conventional methods.

Reaction Kinetics, Mechanisms and Catalysis published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C26H41N5O7S, Safety of 3-Acetyldihydrofuran-2(3H)-one.

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

Fan, Wuhou published the artcileAchieving fast self-healing and reprocessing of supertough water-dispersed “living” supramolecular polymers containing dynamic ditelluride bonds under visible light, Related Products of esters-buliding-blocks, the publication is ACS Applied Materials & Interfaces (2020), 12(5), 6383-6395, database is CAplus and MEDLINE.

It is very challenging to achieve polymers that are mech. robust and fast self-healable at ambient conditions, which are highly desirable for smart materials of the next-generation. Herein, combining dynamic ditelluride bonds and 2-ureido-4[1H]-pyrimidinone (UPy) moieties in the main chains, a novel type of visible-light-induced self-healing water-dispersed supramol. polymers (DTe-WSPs) with outstanding healing properties were developed. The prepared DTe-WSPs emulsions showed excellent emulsion stability, and highly transparent DTe-WSPs films obtained from these emulsions exhibited much improved mech. properties and fast recoverability after the incorporation of UPy groups, owing to the phys. cross-links formed by quadruple hydrogen-bonded UPy moieties. Supertoughness (105.2 MJ m^-3) and fast self-healability under visible light (healing efficiency of 85.6% within 10 min) could be achieved simultaneously with the adjustment of the ditelluride content and the UPy content, and the toughness of our polymers is higher than those of the reported ambient temperature self-healable polymers. The visible-light-induced ditelluride metathesis is a predominant factor in the healing process of DTe-WSPs, and the ditelluride metathesis triggered by photothermy and hydrogen bonding could also afford the ultimate healing result. Meanwhile, DTe-WSPs can be reprocessed using visible light, providing a facile way to process polymers at mild conditions. To our surprise, the “living” DTe-WSPs exhibited the ability to initiate the polymerization of vinyl monomers under visible light, which is first reported for water-dispersed self-healing polymers. We considered the elaborated design philosophy, based on the readily available, clean, safe, and easily manipulated visible light, which can not only provide inspiration for preparing fast ambient temperature self-healing and reprocessing polymer materials with robust mech. properties but also develop a new macroinitiator to initiate the ambient temperature polymerization of vinyl monomers.

ACS Applied Materials & Interfaces published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, Related Products of esters-buliding-blocks.

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

Yuan, Chuan published the artcileStudy on catalytic pyrolysis mechanism of seaweed polysaccharide monomer, SDS of cas: 517-23-7, the publication is Combustion and Flame (2020), 1-11, database is CAplus.

In this study, L-rhamnose monohydrate (LRM) was used as a model compound of seaweed polysaccharide to study its pyrolysis and catalytic pyrolysis mechanism. Initially, the weight loss curve of LRM was obtained by thermogravimetric anal. The main weight loss temperature was found to be at 350-550°C. Then, the pyrolysis mechanism of LRM was analyzed and verified by macroscopic experiments and mol. simulations. Experiments showed that the bio-oil yield was highest when the temperature reached around 500°C, and the bio-oil contained large amount of furan substances. Finally, the effects of different proportions of catalysts (Mg-Ce/ZSM-5) on bio-oil products were studied, and the catalytic reaction mechanism was discussed.

Combustion and Flame published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C4H3Cl2N3, SDS of cas: 517-23-7.

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

Ullah, Mohammad Shahid published the artcileCinchona Squaramide-Based Chiral Polymers as Highly Efficient Catalysts in Asymmetric Michael Addition Reaction, Related Products of esters-buliding-blocks, the publication is ACS Omega (2018), 3(4), 4573-4582, database is CAplus and MEDLINE.

We have synthesized novel chiral polymers containing a cinchona-based squaramide in the main chain. We designed a novel cinchona squaramide dimer that contains two cinchona squaramide units connected by diamines. The olefinic double bonds in the cinchona squaramide dimer were used for Mizoroki-Heck (MH) polymerization with aromatic diiodides. The MH polymerization of the cinchona squaramide dimer and aromatic diiodide proceeded well to give the corresponding chiral polymers in good yields. The catalytic activity of the chiral polymers was investigated for asym. Michael addition reactions. The effect of the squaramide structure of the polymeric catalyst on the catalytic performance is discussed in detail. We have surveyed the influence of the chiral polymer structure on the catalytic activity and enantioselectivity of the asym. reaction. The asym. Michael addition of β-ketoesters to nitroolefins was successfully catalyzed by polymeric cinchona squaramide organocatalysts to obtain the corresponding Michael adducts in good yields with excellent enantio- and diastereoselectivities. The polymeric catalysts were insoluble in commonly used organic solvents and easily recovered from the reaction mixture and reused several times without the loss of catalytic activity.

ACS Omega published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C15H15OP, Related Products of esters-buliding-blocks.

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

Chen, Kai published the artcileEngineered Cytochrome c-Catalyzed Lactone-Carbene B-H Insertion, Computed Properties of 517-23-7, the publication is Synlett (2019), 30(4), 378-382, database is CAplus and MEDLINE.

Previous work has demonstrated that variants of a heme protein, Rhodothermus marinus cytochrome c(Rma cyt c), catalyze abiol. carbene boron-hydrogen (B-H) bond insertion with high efficiency and selectivity. Here authors investigated this carbon-boron bond-forming chem. with cyclic, lactone-based carbenes. Using directed evolution, they obtained a Rma cyt c variant BOR^LAC that shows high selectivity and efficiency for B-H insertion of 5- and 6-membered lactone carbenes (up to 24,500 total turnovers and 97.1:2.9 enantiomeric ratio). The enzyme shows low activity with a 7-membered lactone carbene. Computational studies revealed a highly twisted geometry of the 7-membered lactone carbene intermediate relative to 5- and 6-membered ones. Directed evolution of cytochrome c together with computational characterization of key iron-carbene intermediates has allowed us to expand the scope of enzymic carbene B-H insertion to produce new lactone-based organoborons.

Synlett published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, Computed Properties of 517-23-7.

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

Fan, Cheng-Jie published the artcileA robust self-healing polyurethane elastomer: From H-bonds and stacking interactions to well-defined microphase morphology, COA of Formula: C6H8O3, the publication is Science China Materials (2019), 62(8), 1188-1198, database is CAplus.

Supramol. interactions have been extensively considered in the field of self-healing materials due to their excellent reversibility and sensitive responsiveness to environmental stimuli. However, development of a polymeric material with good mech. performance as well as self-healing capacity is very challenging. In this study, we report a robust self-healing polyurethane (PU) elastomer polypropylene glycol-2-amino-5-(2- hydroxyethyl)-6-methylpyrimidin-4-ol (PPG-mUPy) by integrating ureidopyrimidone (UPy) motifs with a PPG segment with a well-defined architecture and microphase morphol. To balance the self-healing capacity and mech. performance, a thermal-triggered switch of H-bonding is introduced. The quadruple H-bonded UPy dimeric moieties in the backbone induce phase separation to form a hard domain as well as enable further aggregation into microcrystals by virtue of the stacking interactions, which are stable in ambient temperature This feature endows the PU with high mech. strength. Meanwhile, a high healing efficiency can be realized, when the reversibility of the H-bond was unlocked from the stacking at higher temperature An optimized sample PPG₁₀₀₀-mUPy^50% with a good balance of mech. performance (20.62 MPa of tensile strength) and healing efficiency (93% in tensile strength) was achieved. This strategy will provide a new idea for developing robust self-healing polymers.

Science China Materials published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, COA of Formula: C6H8O3.

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

Li, Xin published the artcileEnantio- and diastereoselective diarylmethylation of 1,3-dicarbonyl compounds, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one, the publication is Chemical Science (2020), 11(23), 5969-5973, database is CAplus and MEDLINE.

A Cu-catalyzed enantio- and diastereoselective diarylmethylation of 1,3-dicarbonyl compounds RC(O)CH(R¹)C(O)R² (R = Et, 4-methoxyphenyl, cyclohexyl, thiophen-2-yl, etc.; R¹ = H, Me; R² = Me, OMe, OEt, O(i-Pr); RR¹ = -(CH₂)₃-, -(CH₂)₄-, -(CH₂)₂O-) and Me 1-oxo-2-indancarboxylate is described. It is a successful example of constructing all-carbon quaternary stereocenters from 3°C-H nucleophiles, a challenging topic in synthetic chem. In the present work, two contiguous stereocenters I (R³ = R⁴ = Me, t-Bu, i-Pr, TMS, Ph; R³ = Me, R⁴ = t-Bu; Ar = naphthalen-2-yl, 1-benzofuran-2-yl, 2,3-dihydro-1,4-benzodioxin-6-yl, thiophen-2-yl, etc.) are constructed with high levels of stereoselectivity and atom economy. The broad scope of 1,3-dicarbonyl nucleophiles and the tolerance of a wide range of functional groups make this protocol of great importance in the synthesis of chiral diarylmethane compounds I.

Chemical Science published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one.

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

Wannenmacher, Nick published the artcileDiastereospecific Enantiodivergent Allylation of Pyrazolones as an Entry to β-Aminoamides, Category: esters-buliding-blocks, the publication is Advanced Synthesis & Catalysis, database is CAplus.

A diastereospecific enantiodivergent allylation of pyrazolones I (R¹ = n-Pr, H₂C:CHCH₂, PhCH₂, etc.; R² = Me, i-Pr, Ph; R³ = Ph, PhCH₂, 4-MeOC₆H₄) with allyl imidates R⁴CH:CHCH₂OC(:NH)CCl₃ (R⁴ = Me, n-Pr, PhCH₂CH₂, MeO₂CCH₂CH₂, PhCH₂OCH₂CH₂), catalyzed by a planar chiral pentaphenylferrocene-based palladacycle, is reported. With the same catalyst, both enantiomeric products II were selectively available from (E)- or (Z)-allyl imidates. The method is applicable to structurally diverse substrates and gave products II with 85-94% enantiomeric excesses. In addition, pyrazolone (S,E)-II (R¹ = 4-FC₆H₄CH₂; R² = Me; R³ = Ph; R⁴ = PhCH₂CH₂) was transformed into acyclic β-aminoamide.

Advanced Synthesis & Catalysis published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C13H18BNO3, Category: esters-buliding-blocks.

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

Larsen, Matthew A. published the artcileA Modular and Diastereoselective 5 + 1 Cyclization Approach to N-(Hetero)Aryl Piperidines, HPLC of Formula: 517-23-7, the publication is Journal of the American Chemical Society (2020), 142(2), 726-732, database is CAplus and MEDLINE.

A new general de novo synthesis of pharmaceutically important N-(hetero)aryl piperidines is reported. This protocol uses a robustly diastereoselective reductive amination/aza-Michael reaction sequence to achieve rapid construction of complex polysubstituted ring systems starting from widely available heterocyclic amine nucleophiles and carbonyl electrophiles. Notably, the diastereoselectivity of this process is enhanced by the presence of water, and DFT calculations support a stereochem. model involving a facially selective protonation of a water-coordinated enol intermediate.

Journal of the American Chemical Society published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C6H8O3, HPLC of Formula: 517-23-7.

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

Tran, Van T. published the artcileActivation of diverse carbon-heteroatom and carbon-carbon bonds via palladium(II)-catalyzed β-X elimination, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one, the publication is Nature Chemistry (2018), 10(11), 1126-1133, database is CAplus and MEDLINE.

γ-Substituted N-(8-quinolinyl) alkanecarboxamides and cycloalkanecarboxamides such as I underwent regioselective substitution reactions with nucleophiles such as 1-methyl- and 1,2-dimethylindoles in the presence of Pd(OAc)₂ and 1-adamantanecarboxylic acid (1-AdCO₂H) to yield substitution products such as II (R = H, Me). The substitutions occurred using elimination reactions of the β-palladated carboxamides as a key step; a β-palladation product was isolated and its structure determined by X-ray crystallog. The substitution reactions occurred at alkyl C(sp³)-oxygen, nitrogen, carbon, fluorine and sulfur bonds with high regioselectivity. The method was used for substitution reactions of γ-substituted amino acids such as the 8-aminoquinolinyl amide of L-methionine and its sulfoxide to give functionalized amino acids in 60-98% ee. Unstrained 8-aminoquinolinyl heterocyclylalkanecarboxamides underwent regioselective γ-substitution reactions with ring opening if a heteroatom was in the γ-position; if the heteroatom was in an appropriate position, lactonization and lactamization reactions also occurred with loss of the aminoquinoline moieties.

Nature Chemistry published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C18H28B2O4, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one.

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