Category: 107-54-0

Wu, Yao published the artcileA Copper Iodide Cluster-Based Metal-Organic Polyhedra for Photocatalytic Click Chemistry, Product Details of C8H14O, the main research area is phenyl triazole preparation click chem; aryl acetylene benzyl azide alkyne cycloaddition copper iodide photocatalyst.

Herein, a copper(I) iodide cluster-based metal-organic polyhedra (Cu3I3)4L14 (1) ((L1 = 1,3,5-trispyridylsulfanylethyl)-2,4,6-triethylbenzene, 2-mercaptopyridine) is synthesized. Due to the abnormal geometry of [Cu3I3] SBUs, MOP 1 exhibits a half-truncated cube topol., which is rarely observed up to date. Compared with commonly used metal ion or clusters, the coordination bond between the [Cu3I3] SBU and the ligand is rather labile in solution evidenced by the theor. calculations and exptl. results. Interestingly, the liable [Cu3I3] SBU endows MOP 1 to photocatalyze the azide-alkyne cycloaddition reaction in aqueous solution with high efficiency, excellent tolerance (>80% isolated yield for 18 examples), and good recyclability. The mechanistic studies reveal a photoinduced electron transfer from the MOP to azide, which is unusual in copper-catalyzed click reactions.

Small Structures published new progress about 1,3-Dipolar cycloaddition catalysts (azide-alkyne, regioselective). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, Product Details of C8H14O.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Islam, Sk Safikul published the artcileZinc (II) incorporated porous organic polymeric material (POPs): A mild and efficient catalyst for synthesis of dicoumarols and carboxylative cyclization of propargyl alcohols and CO2 in ambient conditions, Recommanded Product: 3,5-Dimethylhex-1-yn-3-ol, the main research area is dicoumarol preparation green chem; hydroxycoumarin aryl aldehyde condensation zinc catalyst; alkylidene cyclic carbonate preparation green chem; propargyl alc carbon dioxide cyclization reaction zinc catalyst.

Zinc (II) incorporated porous organic polymer catalyst, Zn@BBAPA has been designed, synthesized and characterized thoroughly by XRD, EDX, SEM, HR-TEM, FTIR spectra, UV-vis spectra, TGA and N2 absorption desorption isotherm. An eco-friendly porous Zn@BBAPA catalyst exhibits highly efficient catalytic performance for the production of α-alkylidene cyclic carbonates I (R1 = Me; R2 = Me, Et, isobutyl; R1R2 = -(CH2)5-) by using propargylic alcs. HCCC(R1)(R2)OH via CO2 fixation. In addition the catalyst shows outstanding efficiency for the synthesis of various dicoumarol derivatives II (R3 = 4-methoxyphenyl, furan-2-yl, thiophen-2-yl, etc.) in green solvent medium (water) from 4-hydroxycoumarin and aromatic aldehydes R3CHO. Presence of super hydrophobic nature and electron-donation character of NH2 groups of BBA framework with high surface area is main aspect to be responsible for elevated catalytic performance as well as improvement in catalyst stability and enabling a good recyclability.

Molecular Catalysis published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, Recommanded Product: 3,5-Dimethylhex-1-yn-3-ol.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Zhou, Zhi-Hua published the artcileSynthesis of α-hydroxy ketones by copper(I)-catalyzed hydration of propargylic alcohols: CO2 as a cocatalyst under atmospheric pressure, Synthetic Route of 107-54-0, the main research area is hydroxy ketone preparation; propargylic alc hydration copper carbon dioxide cocatalyst.

Inexpensive and efficient Cu(I) catalysis is reported for the synthesis of α-hydroxy ketones CH3C(O)C(R1)(R2)OH [R1 = Me, Et, iso-Bu, hexyl, vinyl; R2 = Me, phenyl; R1R2 = -(CH2)5-] and 17β-hydroxyprogesterone from propargylic alcs. HCCC(R1)(R2)OH and 17β-hydroxypregn-5-en-20-yn-3-one, CO2, and water via tandem carboxylative cyclization and nucleophilic addition reaction. Notably, hydration of propargylic alcs. can be carried out smoothly under atm. CO2 pressure, generating a series of α-hydroxy ketones efficiently and selectively. This strategy shows great potential for the preparation of valuable α-hydroxy ketones by using CO2 as a crucial cocatalyst under mild conditions.

Chinese Journal of Catalysis published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, Synthetic Route of 107-54-0.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Yuan, Ye published the artcileA green and recyclable CuSO4·5H2O/ionic liquid catalytic system for the CO2-promoted hydration of propargyl alcohols: an efficient assembly of α-hydroxy ketones, Related Products of alcohols-buliding-blocks, the main research area is propargyl alc copper ionic liquid hydration reaction green chem; alpha hydroxy ketone preparation.

In this work, diverse α-hydroxy ketones were efficiently constructed through the CO2-promoted hydration process of propargyl alcs., which was catalyzed by a system consisted of economical CuSO4·5H2O and a green 1-butyl-3-methylimidazolium acetate ionic liquid Particularly, this catalytic system exhibited excellent activity under atm. CO2 or even mimetic flue gas (20 vol% of CO2). Moreover, this system employed the lowest metal loading ever reported (0.004-0.25 mol%) meanwhile reached the highest turnover number (11700) for the target hydration reaction. Addnl., this was the first reported Cu catalytic system with reliable recyclability, which could be easily reused at least 6 times with yields higher than 85%.

Journal of Catalysis published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, Related Products of alcohols-buliding-blocks.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Zhang, Yongxing published the artcileCO2-induced dissolution of ZnO into ionic liquids and its catalytic application for the hydration of propargylic alcohols, SDS of cas: 107-54-0, the main research area is propargylic alc ionic liquid zinc catalyst hydration green chem; hydroxyketone preparation.

An unexpected CO2-induced dissolution of ZnO into ionic liquids was discovered. This process exhibited high dissolution speed and the dissociated mixture was applied as an efficient Zn-based catalytic system for the CO2-promoted hydration of propargylic alcs. under atm. pressure with broad substrate scope. Moreover, this system was recycled and reused for at least 16 times with excellent yields continuously obtained, which was an unprecedented record for this reaction. Significantly, this system could employ waste pigments as the ZnO source and work even under flue gas atm. In the mechanistic investigations, the interaction between ZnO, CO2 and ionic liquids to give N-heterocyclic carbene/CO2 adducts proved to be the key factor for this specific dissolution These adducts were further identified to exhibit better reactivity than the normal CO2 by exptl. data and d. functional theory (DFT) calculations, which might be responsible for the excellent performance of the abovementioned catalytic system.

Applied Catalysis, B: Environmental published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, SDS of cas: 107-54-0.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Hou, Sheng-Li published the artcileA Noble-Metal-Free Metal-Organic Framework (MOF) Catalyst for the Highly Efficient Conversion of CO2 with Propargylic Alcohols, Recommanded Product: 3,5-Dimethylhex-1-yn-3-ol, the main research area is MOF catalyst carbon dioxide propargylic alc cyclization; copper iodide indium aminonicotinic acid MOF catalyst; carbon dioxide fixation; cyclizations; heterogeneous catalysis; metal-organic frameworks (MOFs); noble-metal-free.

Cyclization of propargylic alcs. with CO2 is an important reaction in industry, and noble-metal catalysts are often employed to ensure the high product yields under environmentally friendly conditions. Herein a porous noble-metal-free framework {(NH2C2H6)0.75[Cu4I4·(L)3·(In)0.75]·DMF·H2O} (L- 5-aminonicotinic acid) with large 1D channels of 1.66 nm diameter was synthesized for this reaction. Compound {(NH2C2H6)0.75[Cu4I4·(L)3·(In)0.75]·DMF·H2O} exhibits excellent acid/base stability, and is even stable in corrosive triethylamine for one month. Catalytic studies indicate that {(NH2C2H6)0.75[Cu4I4·(L)3·(In)0.75]·DMF·H2O} is an effective catalyst for the cyclization of propargylic alcs. and CO2 without any solvents under mild conditions, and the turnover number (TON) can reach to a record value of 14,400. Furthermore, this MOF catalyst also has rarely seen catalytic activity when the biol. macromol. ethisterone was used as a substrate. Mechanistic studies reveal that the synergistic catalytic effect between CuI and InIII plays a key role in the conversion of CO2.

Angewandte Chemie, International Edition published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, Recommanded Product: 3,5-Dimethylhex-1-yn-3-ol.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Wu, Zhilei published the artcileCopper(I) iodide cluster-based lanthanide organic frameworks: synthesis and application as efficient catalysts for carboxylative cyclization of propargyl alcohols with CO2 under mild conditions, Synthetic Route of 107-54-0, the main research area is dysprosium copper nicotinate metal organic framework preparation crystal structure; gadolinium copper isonicotinate metal organic framework preparation crystal structure; carboxylative cyclization propargyl alc carbon dioxide lanthanide MOF catalyzed.

Two metal-organic frameworks (MOFs), namely, [Dy2Cu4I4(NA)6(DMF)2]n (1) and [Gd2Cu2I2(IN)6(DMF)4]·5DMF (2) (HNA = nicotinic acid, HIN = isonicotinic acid), constructed based on lanthanide ions and copper iodide clusters ([Cu4I4] and [Cu2I2]) were successfully synthesized and characterized. Compound 1 has a three-dimensional framework and compound 2 displays a two-dimensional plane with sql topol., resp. Both of them exhibit high thermostability and solvent stabilities. Addnl., catalytic explorations reveal that 1 displays higher catalytic activity than 2 for the carboxylic cyclization of propargyl alcs. More importantly, 1 also exhibits excellent catalytic performance in the carboxylation reactions of CO2 and terminal propargylic alcs. with various substituents. To the best of authors knowledge, this is the first example of non-noble metal based MOF catalysts for the carboxylative cyclization of propargyl alcs. with CO2 under atm. pressure and at room temperature, which provides a highly promising approach for MOFs in the catalytic conversion of CO2 to valuable chems.

Dalton Transactions published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, Synthetic Route of 107-54-0.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Das, Rajesh published the artcileHighly Efficient Fixation of Carbon Dioxide at RT and Atmospheric Pressure Conditions: Influence of Polar Functionality on Selective Capture and Conversion of CO2, COA of Formula: C8H14O, the main research area is carbon dioxide fixation room temperature polar functionality influence; oxazolidione preparation cyclic carboxylation alkyne porous MOF catalyst.

The rapid increase in the concentration of atm. carbon dioxide (CO2) has resulted in undesirable environmental issues. Hence, selective CO2 capture and utilization as C1 feedstock for the preparation of high-value chems. and fuels has been considered as a promising step toward mitigating the growing concentration of atm. CO2. In this direction, herein we report rational construction of a Ag(I)-anchored sulfonate-functionalized UiO-66 MOF named as MOF-SO3Ag composed of CO2-philic sulfonate functionality and catalytically active alkynophilic Ag(I) sites for chem. fixation of carbon dioxide. The MOF-SO3Ag exhibits selective as well as recyclable adsorption of CO2 with a high heat of adsorption energy (Qst) of 37.8 kJ/mol. On the other hand, the analogous MOF, UiO-66 doped with Ag(I), showed a lower Qst value of 30 kJ/mol, highlighting the importance of the sulfonate group for stronger interaction with CO2. Furthermore, the MOF-SO3Ag acts as an efficient heterogeneous catalyst for cyclic carboxylation of propargylic alcs. to generate α-alkylidene cyclic carbonates in >99% yield at mild conditions of RT and 1 bar CO2. More importantly, one-pot synthesis of oxazolidinones by a three-component reaction between CO2, propargylic alc., and primary amine has also been achieved using MOF-SO3Ag catalyst under the mild conditions. The MOF is highly recyclable and retains its superior catalytic activity even after several cycles. To the best of our knowledge, MOF-SO3Ag is the first example of MOF reported for RT chem. fixation of CO2 to oxazolidinones by aminolysis of α-alkylidene cyclic carbonates under the environment-friendly mild conditions. An efficient chem. fixation of CO2 into high-value chems., α-alkylidene cyclic carbonates, and oxazolidinones by cyclic carboxylation of alkyne mols. with CO2 catalyzed by Ag(I) anchored porous MOF under environment-friendly mild conditions of RT and atm. pressure of CO2 is presented. This work demonstrates the potential application of porous MOFs with pores functionalized with polar functionality for selective carbon capture and utilization (CCU) for synthesis of high-value chems.

Inorganic Chemistry published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, COA of Formula: C8H14O.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Li, Jing-Yuan published the artcileCascade Strategy for Atmospheric Pressure CO2 Fixation to Cyclic Carbonates via Silver Sulfadiazine and Et4NBr Synergistic Catalysis, Application of 3,5-Dimethylhex-1-yn-3-ol, the main research area is cyclic carbonate preparation; hydroxyketone preparation; carbon dioxide diol propargyl alc cascade fixation synergistic catalyst.

It is of great significance and challenge for highly efficient catalytic transformation of carbon dioxide into cyclic carbonates especially under low pressure and energy input conditions. In this regard, an efficient silver sulfadiazine/Et4NBr synergistic catalytic system was developed for the three-component cascade reaction of propargylic alcs., CO2, and vicinal diols. The reaction was performed in the absence of any solvent under atm. CO2 pressure to afford splendid yields of cyclic carbonates. The excellent performance was ascribed to the simultaneous activation of hydroxyl group in propargylic alcs./vicinal diols by silver sulfadiazine and synergistic effect between silver species and bulkier Et4N+ in the procedure of intramol. nucleophilic cyclization confirmed by control experiments and NMR spectra.

ACS Sustainable Chemistry & Engineering published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, Application of 3,5-Dimethylhex-1-yn-3-ol.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Fan, Liqun published the artcileCo-immobilization of Laccase and TEMPO onto Glycidyloxypropyl Functionalized Fibrous Phosphosilicate Nanoparticles for Fixing CO2 into β-Oxopropylcarbamatesin, Application of 3,5-Dimethylhex-1-yn-3-ol, the main research area is alc carbon dioxide amine nanocatalyst laccase TEMPO green fixation; oxopropylcarbamate one pot preparation.

TEMPO or Anchoring 2,2,6,6-tetra-methylpiperidine-1oxyl radical into the nanospaces a fiber of phosphosilicate with laccase compound causes an unheard potent to be producing which called bifunctional nanocatalyst (TEMPO@FPS-laccase). TEMPO@FPS-laccase indicated proper catalytic activity for synthesis of β-oxopropylcarbamates in aqueous medium without any pollutants through a multi component coupling of CO2, amines and propargyl alcs. in moderate condition. Free laccases may not be recovered but can be easily disabled in different environmental conditions. Enzyme immobilization is known as an expanding way to enhance resistor to extreme conditions and stability as well as recycled of laccase.

Catalysis Letters published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 107-54-0 belongs to class alcohols-buliding-blocks, name is 3,5-Dimethylhex-1-yn-3-ol, and the molecular formula is C8H14O, Application of 3,5-Dimethylhex-1-yn-3-ol.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts